510(k) Report

510(k) · Cleared

Cleared

EHC400 Desktop Patient Station; ECH600 Care Provider Station

K003257510(k) TraditionalCleared Dec 22, 200065-day reviewClass II21 CFR 862.1345

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

Cybercare Technologies, Inc. · CGA Glucose Oxidase, Glucose

Cleared on Dec 22, 2000 after a 65-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 11 later devices descend from it.

Decided
Dec 22, 2000
Review
65 days
Class
Class II
Product code
CGA
Recalls
None
Predicates
0

11 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2003: 1 descendant cleared2005: 2 descendants cleared2004: 1 descendant cleared2007: 1 descendant cleared2016: 1 descendant cleared2024: 1 descendant cleared2012: 1 descendant cleared2015: 1 descendant cleared2010: 1 descendant cleared2017: 1 descendant cleared200020052010201520202025
  1. This deviceK003257 EHC400 Desktop Patient Station; ECH600 Care Provider StationCybercare Technologies, Inc. · 2000
  2. Descendant · cites it directly · 10 of its ownK020534 Medstar System, Models 533-300Cybernet Medical · 2003 · Recalled
  3. Descendant · 2 generations on · 8 of its ownK041854 MPM SystemAerotel Medical Systems, Ltd. · 2004
  4. Descendant · 2 generations on · 7 of its ownK051544 Vitalcaregiving SystemAdvanced Monitoring Caregiving, Inc. · 2005
  5. Descendant · 3 generations on · 4 of its ownK063008 Health Check KioskXperex Corporation · 2007
  6. Descendant · 3 generations on · 1 of its ownK151839 AMC Health VitalCaregiving SystemAmc Health · 2016

Showing 5 of 11 descendants. See all descendants

Descendants cleared per year

2003: 12004: 12005: 22007: 12010: 12012: 12015: 12016: 12017: 12024: 1
2003high 2 (2005) · low 0 (2006)2026

Most influential descendants

Showing 5 of 11 · See all
  • K020534Medstar System, Models 533-300Cybernet Medical · 2003 · cites it directly10descendants
  • K041854MPM SystemAerotel Medical Systems, Ltd. · 2004 · 2 generations on8descendants
  • K051544Vitalcaregiving SystemAdvanced Monitoring Caregiving, Inc. · 2005 · 2 generations on7descendants
  • K063008Health Check KioskXperex Corporation · 2007 · 3 generations on4descendants
  • K151839AMC Health VitalCaregiving SystemAmc Health · 2016 · 3 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K003257EHC400 Desktop Patient Station; ECH600 Care Provider StationCybercare Technologies, Inc.2000—
+1K020534Medstar System, Models 533-300Cybernet Medical20034
+2K041854MPM SystemAerotel Medical Systems, Ltd.2004—
+2K051544Vitalcaregiving SystemAdvanced Monitoring Caregiving, Inc.2005—
+3K063008Health Check KioskXperex Corporation2007—
+3K151839AMC Health VitalCaregiving SystemAmc Health2016—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200310
200410
200520
200710
201010
201210
201510
201610
201710
202410
FIG. 1 — Lineage of K003257, 2000–2024Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in CGA? 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 CGA device

  1. #1 K252488 ABL90 FLEX PLUS Systemscore 12.8 · 6 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (11)

See all 11

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K020534Medstar System, Models 533-300Cybernet Medical200310

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?

  • Of its descendants, K020534 (Cybernet Medical, 2003) has gone furthest, with 10 descendants of its own.

How does its category compare?

All CGA devices

CGA Glucose Oxidase, Glucose: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · CGA

2in 2024

2007: 72008: 62009: 102010: 82011: 92012: 102013: 32014: 52015: 42016: 42017: 22018: 22019: 22020: 22021: 12022: 12023: 42024: 22026 (partial year): 1
2007high 10 (2009) · low 0 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CGA

249in 2023

2007: 122 days median2008: 56 days median2009: 155 days median2010: 122 days median2011: 217 days median2012: 123 days median2013: 441 days median2014: 265 days median2015: 150 days median2016: 157 days median2023: 249 days median
2007high 441 (2013) · low 56 (2008)2026

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

Recalls per year · CGA

3in 2023

2007: 22008: 22009: 42010: 62011: 32013: 32014: 22015: 6, 2 Class I2016: 22019: 12023: 3
2007high 6 (2010) · low 0 (2012)2026

Class I (2 since 2007) Class II/III not classified

Adverse event reports per year · CGA

59in 2025

2007: 292008: 372009: 752010: 1722011: 4232012: 2332013: 1722014: 1222015: 1552016: 362017: 922018: 692019: 1162020: 682021: 482022: 2722023: 1,1412024: 2662025: 59
2007high 1,141 (2023) · low 29 (2007)2025

MAUDE reports naming product code CGA, 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
20077122229
2008656237
200910155475
201081226172
201192173423
2012101230233
201334413172
201452652122
201541506 (2)155
20164157236
20172—092
20182—069
20192—1116
20202—068
20211—048
20221—0272
2023424931,141
20242—0266
20250—059
20261—0—
Cite this page

510(k) Report. “K003257: EHC400 Desktop Patient Station; ECH600 Care Provider Station.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K003257

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026