510(k) Report

510(k) · Cleared

Cleared

Intel Health Guide, Model: PHS6000

K080798510(k) AbbreviatedCleared Jun 27, 200899-day reviewClass II21 CFR 870.2910

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Intel Corp. · DRG Transmitters And Receivers, Physiological Signal, Radiofrequency

Cleared on Jun 27, 2008 as substantially equivalent to K023749 (Philips Medical Systems, 2002) and 2 other predicates after a 99-day review. Its family tree reaches back 11 generations to 1987. 25 later devices descend from it.

Decided
Jun 27, 2008
Review
99 days
Class
Class II
Product code
DRG
Recalls
None
Predicates
3

Its longest line of descent runs back 11 generations to K864318 (1987). 50 ancestors in all, the oldest K790130 (1979). 25 later devices descend from it, 10 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2004: 3 other ancestors2003: 3 other ancestors1999: 5 other ancestors2002: 2 other ancestors2001: 4 other ancestors2000: 2 other ancestors1998: 4 other ancestors1997: 2 other ancestors1996: 2 other ancestors1995: 3 other ancestors1979: 1 other ancestor1993: 2 other ancestors1990: 1 other ancestor1987: 2 other ancestors1988: 1 other ancestor1992: 1 other ancestor1991: 1 other ancestor2011: 6 descendants cleared2013: 6 descendants cleared2009: 1 descendant cleared2008: 1 descendant cleared2010: 1 descendant cleared2014: 2 descendants cleared2012: 3 descendants cleared2018: 1 descendant cleared2017: 1 descendant cleared2020: 1 descendant cleared2022: 1 descendant cleared2025: 1 descendant clearedK864318 · The Buddy System/Health Information System · The Buddy Systems, Inc. · 1987K952979 · Hanc Network · Healthtech Services Corp. · 1996K964408 · Poseidon Cardiac Monitoring System (PCMS) · Instromedix, Inc. · 1997K993169 · Modification of: Physiological Signal Transmitter and Receiver, Model 3810A · Hewlett-Packard Co. · 1999K023749 · The M3810A Philips Telemonitoring System with M3812B Telestation (M310A/12B) · Philips Medical Systems · 2002K031840 · Carematix Wellness System · Carematix, Inc. · 2003×2: 2 generations cleared close together, K040966 (2004), K042273 (2004) K050567 · Health Buddy Appliance · Health Hero Network, Inc. · 2005K060843 · Modification to Health Buddy Appliance · Health Hero Network, Inc. · 2006K063612 · Modification to Health Buddy Appliance · Health Hero Network, Inc. · 200619801990200020102020
  1. Root · 11 generations backK864318 The Buddy System/Health Information SystemThe Buddy Systems, Inc. · 1987
  2. 7 generations between
  3. 3 generations backK050567 Health Buddy ApplianceHealth Hero Network, Inc. · 2005
  4. 2 generations backK060843 Modification to Health Buddy ApplianceHealth Hero Network, Inc. · 2006
  5. 1 generation backK063612 Modification to Health Buddy ApplianceHealth Hero Network, Inc. · 2006
  6. This deviceK080798 Intel Health Guide, Model: PHS6000Intel Corp. · 2008
  7. Descendant · cites it directly · 12 of its ownK083862 Medapps 2.0 Remote Patient Monitoring SystemMedapps, Inc. · 2009
  8. Descendant · cites it directly · 12 of its ownK083115 Modification to Intel Health Guide, Model PHS6000Intel Corp. · 2008
  9. Descendant · cites it directly · 11 of its ownK101178 Modification to Intel Health Guide PHS6000Intel Corp. · 2010
  10. Descendant · cites it directly · 10 of its ownK103276 Intel Health GuideIntel Corporation Digital Health Group · 2011
  11. Descendant · 2 generations on · 5 of its ownK122285 Tablet CommanderCardiocom, LLC · 2012
Show all 11 generations
  1. Root · 11 generations backK864318 The Buddy System/Health Information SystemThe Buddy Systems, Inc. · 1987
  2. 10 generations backK952979 Hanc NetworkHealthtech Services Corp. · 1996
  3. 9 generations backK964408 Poseidon Cardiac Monitoring System (PCMS)Instromedix, Inc. · 1997
  4. 8 generations backK993169 Modification of: Physiological Signal Transmitter and Receiver…Hewlett-Packard Co. · 1999
  5. 7 generations backK023749 The M3810A Philips Telemonitoring System with M3812B Telestation…Philips Medical Systems · 2002
  6. 6 generations backK031840 Carematix Wellness SystemCarematix, Inc. · 2003
  7. 5 generations backK040966 Modification to Carematix Wellness SystemCarematix, Inc. · 2004
  8. 4 generations backK042273 Modification to Health Buddy with Device ConnectivityHealth Hero Network, Inc. · 2004
  9. 3 generations backK050567 Health Buddy ApplianceHealth Hero Network, Inc. · 2005
  10. 2 generations backK060843 Modification to Health Buddy ApplianceHealth Hero Network, Inc. · 2006
  11. 1 generation backK063612 Modification to Health Buddy ApplianceHealth Hero Network, Inc. · 2006
  12. This deviceK080798 Intel Health Guide, Model: PHS6000Intel Corp. · 2008

Showing 5 of 25 descendants. See all descendants

Descendants cleared per year

2008: 12009: 12010: 12011: 62012: 32013: 62014: 22017: 12018: 12020: 12022: 12025: 1
2008high 6 (2011) · low 0 (2015)2026

Most influential descendants

Showing 5 of 25 · See all
  • K083862Medapps 2.0 Remote Patient Monitoring SystemMedapps, Inc. · 2009 · cites it directly12descendants
  • K083115Modification to Intel Health Guide, Model PHS6000Intel Corp. · 2008 · cites it directly12descendants
  • K101178Modification to Intel Health Guide PHS6000Intel Corp. · 2010 · cites it directly11descendants
  • K103276Intel Health GuideIntel Corporation Digital Health Group · 2011 · cites it directly10descendants
  • K122285Tablet CommanderCardiocom, LLC · 2012 · 2 generations on5descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−11K864318The Buddy System/Health Information SystemThe Buddy Systems, Inc.1987—
−10K952979Hanc NetworkHealthtech Services Corp.1996—
−9K964408Poseidon Cardiac Monitoring System (PCMS)Instromedix, Inc.1997—
−8K993169Modification of: Physiological Signal Transmitter and Receiver, Model 3810AHewlett-Packard Co.1999—
−7K023749The M3810A Philips Telemonitoring System with M3812B Telestation (M310A/12B)Philips Medical Systems2002—
−6K031840Carematix Wellness SystemCarematix, Inc.2003—
−5K040966Modification to Carematix Wellness SystemCarematix, Inc.2004—
−4K042273Modification to Health Buddy with Device ConnectivityHealth Hero Network, Inc.2004—
−3K050567Health Buddy ApplianceHealth Hero Network, Inc.2005—
−2K060843Modification to Health Buddy ApplianceHealth Hero Network, Inc.2006—
−1K063612Modification to Health Buddy ApplianceHealth Hero Network, Inc.2006—
0 (this device)K080798Intel Health Guide, Model: PHS6000Intel Corp.2008—
+1K083862Medapps 2.0 Remote Patient Monitoring SystemMedapps, Inc.2009—
+1K083115Modification to Intel Health Guide, Model PHS6000Intel Corp.2008—
+1K101178Modification to Intel Health Guide PHS6000Intel Corp.2010—
+1K103276Intel Health GuideIntel Corporation Digital Health Group2011—
+2K122285Tablet CommanderCardiocom, LLC2012—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197910
198720
198810
199010
199110
199210
199320
199530
199620
199720
199840
199950
200020
200140
200220
200330
200430

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200810
200910
201010
201160
201230
201360
201420
201710
201810
202010
202210
202510
FIG. 1 — Lineage of K080798, 1987–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in DRG? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new DRG device

  1. #1 K223711 ANNE Onescore 20.8 · 11 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (4)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K023749The M3810A Philips Telemonitoring System with M3812B Telestation (M310A/12B)
Summary page 1
…910, Product Code DRG) Substantial Equivalence is claimed to the following devices: 1. Philips Medical Systems' M3810A TeleMonitoring System with M3812B TeleStation (K023749) ~ 2. Health Hero Network's Health Buddy' Appliance (K063612)…
Philips Medical Systems2002—
*K063612Modification to Health Buddy Appliance
Summary page 1
…Systems' M3810A TeleMonitoring System with M3812B TeleStation (K023749) ~ 2. Health Hero Network's Health Buddy' Appliance (K063612) TM Patient Monitoring system (K041308) 3. WEBVMC. LLC's RemoteNurse Device Description The…
Health Hero Network, Inc.2006—
*K041308Remotenurse Patient Monitoring System
Summary page 1
…~ 2. Health Hero Network's Health Buddy' Appliance (K063612) TM Patient Monitoring system (K041308) 3. WEBVMC. LLC's RemoteNurse Device Description The Intel ' IHealth Guide PHS6000 is a communication tool that allows caregiver…
Webvmc, LLC2004—
*—WEBVMC, LLC's RemoteNurse
Named without a submission number
—

Also cleared against K023749: 9 other devices →

What descends from it? (25)

See all 25

10 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K083862Medapps 2.0 Remote Patient Monitoring SystemMedapps, Inc.200912
K083115Modification to Intel Health Guide, Model PHS6000Intel Corp.200812
K101178Modification to Intel Health Guide PHS6000Intel Corp.201011
K103276Intel Health GuideIntel Corporation Digital Health Group201110
K124000Medapps 2.0 - Remote Patient Monitoring SystemMedapps Inc., Dba Alere Connect20134
K112559Medapps 2.0 Remote Patient Monitoring SystemMedapps, Inc.20114
K130676Ambio Remote Health Monitoring SystemArrayent Health, LLC D/B/A Ambio Health20131
K103796Telemedcare Health MonitorTelemedcare Pty, Ltd.20111
K110334Waldo Patient MonitorWaldo Health20111
K111922Vocare Myhealth TabletVocare, Inc.20110

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 21 years and passes through 8 companies; a new generation was cleared every 12 months on median.
  • 6 of the 50 ancestors have a recall of any class.
  • Of its descendants, K083862 (Medapps, Inc., 2009) has gone furthest, with 12 descendants of its own.
  • 9 other devices also cite its predicate K023749.

How does its category compare?

All DRG devices

DRG Transmitters And Receivers, Physiological Signal, Radiofrequency: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · DRG

3in 2025

2007: 62008: 52009: 132010: 102011: 92012: 122013: 132014: 102015: 22016: 22017: 72018: 62019: 52020: 62021: 22022: 62023: 42024: 32025: 32026 (partial year): 2
2007high 13 (2009) · low 2 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DRG

127in 2025

2007: 63 days median2008: 74 days median2009: 94 days median2010: 68 days median2011: 104 days median2012: 103 days median2013: 146 days median2014: 177 days median2017: 98 days median2018: 220 days median2019: 122 days median2020: 159 days median2022: 287 days median2023: 212 days median2024: 125 days median2025: 127 days median
2007high 287 (2022) · low 63 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · DRG

3in 2007

2007: 32026 (partial year): 1
2007high 3 (2007) · low 0 (2008)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · DRG

52in 2025

2007: 142008: 92009: 52010: 132011: 122012: 92013: 132014: 972015: 1312016: 1822017: 4842018: 1662019: 702020: 822021: 1072022: 432023: 192024: 262025: 52
2007high 484 (2017) · low 5 (2009)2025

MAUDE reports naming product code DRG, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007663314
200857409
2009139405
20101068013
20119104012
20121210309
201313146013
201410177097
20152—0131
20162—0182
20177980484
201862200166
20195122070
20206159082
20212—0107
20226287043
20234212019
20243125026
20253127052
20262—1—

What is it indicated for?

The Intel Health Guide PHS6000 is a communication tool that allows caregivers to remotely access vital sign measurements of patients at home. It collects measurements captured on commercially available wireless or tethered medical devices designed for home use, stores and displays the collected information on the LCD screen, and transmits the information to a secure host server. Caregivers can review the transmitted information and select education and…

Read the full statement (196 words)

The Intel Health Guide PHS6000 is a communication tool that allows caregivers to remotely access vital sign measurements of patients at home. It collects measurements captured on commercially available wireless or tethered medical devices designed for home use, stores and displays the collected information on the LCD screen, and transmits the information to a secure host server. Caregivers can review the transmitted information and select education and reminders for patients using a caregiver software interface to the host server. Patients can review the stored vital sign measurement information and receive educational and motivational content from caregivers. Patients can also optionally engage in video conferences with caregivers and answer the caregivers' questions by participating in surveys.

The Intel Health Guide PHS6000 is not intended for diagnosis or as a substitute for medical care, and it is not intended to provide real time data. It is made available to patients when time-critical care is not required. It is contraindicated for patients requiring direct medical supervision or emergency intervention. It is intended for patients who are willing and capable of managing its use. Clinical judgment and experience by a caregiver are required to check and interpret the information delivered.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K080798: Intel Health Guide, Model: PHS6000.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K080798

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026