510(k) Report

510(k) · Cleared

Cleared

Mortara Instrument ST Central Station

K922927510(k) TraditionalCleared Nov 10, 1992146-day reviewClass II21 CFR 870.2340

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

Mortara Instrument, Inc. · DPS Electrocardiograph

Cleared on Nov 10, 1992 after a 146-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 12 later devices descend from it.

Decided
Nov 10, 1992
Review
146 days
Class
Class II
Product code
DPS
Recalls
None
Predicates
0

12 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2006: 1 descendant cleared1997: 1 descendant cleared2013: 2 descendants cleared2017: 2 descendants cleared2014: 2 descendants cleared2022: 1 descendant cleared2018: 2 descendants cleared2020: 1 descendant cleared1990200020102020
  1. This deviceK922927 Mortara Instrument ST Central StationMortara Instrument, Inc. · 1992
  2. Descendant · cites it directly · 10 of its ownK060135 Mortara Surveyor Telemetry Central StationMortara Instrument, Inc. · 2006
  3. Descendant · 2 generations on · 6 of its ownK131929 Surveyor Central StationMortara Instrument, Inc. · 2013
  4. Descendant · 3 generations on · 3 of its ownK133973 Tempus Pro with Enhanced FeaturesRemote Diagnostic Technologies, Ltd. · 2014
  5. Descendant · 4 generations on · 2 of its ownK170567 Tempus Pro Patient MonitorRemote Diagnostic Technologies, Ltd. · 2017
  6. Descendant · 2 generations on · 2 of its ownK123556 Mortara Surveyor Patient MonitorMortara Instrument, Inc. · 2013 · Recalled

Showing 5 of 12 descendants. See all descendants

Descendants cleared per year

1997: 12006: 12013: 22014: 22017: 22018: 22020: 12022: 1
1997high 2 (2013) · low 0 (1998)2026

Most influential descendants

Showing 5 of 12 · See all
  • K060135Mortara Surveyor Telemetry Central StationMortara Instrument, Inc. · 2006 · cites it directly10descendants
  • K131929Surveyor Central StationMortara Instrument, Inc. · 2013 · 2 generations on6descendants
  • K133973Tempus Pro with Enhanced FeaturesRemote Diagnostic Technologies, Ltd. · 2014 · 3 generations on3descendants
  • K170567Tempus Pro Patient MonitorRemote Diagnostic Technologies, Ltd. · 2017 · 4 generations on2descendants
  • K123556Mortara Surveyor Patient MonitorMortara Instrument, Inc. · 2013 · 2 generations on2descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K922927Mortara Instrument ST Central StationMortara Instrument, Inc.1992—
+1K060135Mortara Surveyor Telemetry Central StationMortara Instrument, Inc.2006—
+2K131929Surveyor Central StationMortara Instrument, Inc.2013—
+3K133973Tempus Pro with Enhanced FeaturesRemote Diagnostic Technologies, Ltd.2014—
+4K170567Tempus Pro Patient MonitorRemote Diagnostic Technologies, Ltd.2017—
+2K123556Mortara Surveyor Patient MonitorMortara Instrument, Inc.20131

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199710
200610
201320
201420
201720
201820
202010
202210
FIG. 1 — Lineage of K922927, 1992–2022Source: 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 DPS? 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 DPS device

  1. #1 K212112 Cardiologs Holter Platformscore 18.6 · 5 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?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (12)

See all 12

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

NumberDeviceApplicantDecidedDescendants
K060135Mortara Surveyor Telemetry Central StationMortara Instrument, Inc.200610
K942685Ecg Review StationMortara Instrument, Inc.19970

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, K060135 (Mortara Instrument, Inc., 2006) has gone furthest, with 10 descendants of its own.

How does its category compare?

All DPS devices

DPS Electrocardiograph: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · DPS

6in 2025

2007: 112008: 132009: 142010: 112011: 222012: 122013: 102014: 112015: 82016: 112017: 92018: 142019: 32020: 62021: 52022: 62023: 102024: 82025: 62026 (partial year): 6
2007high 22 (2011) · low 3 (2019)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DPS

163in 2025

2007: 87 days median2008: 31 days median2009: 84 days median2010: 104 days median2011: 154 days median2012: 117 days median2013: 134 days median2014: 253 days median2015: 178 days median2016: 229 days median2017: 177 days median2018: 221 days median2019: 178 days median2020: 224 days median2021: 135 days median2022: 244 days median2023: 236 days median2024: 260 days median2025: 163 days median2026 (partial year): 258 days median
2007high 260 (2024) · low 31 (2008)2026

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

Recalls per year · DPS

3in 2025

2007: 22009: 12010: 22011: 12019: 92020: 22021: 12022: 12023: 32024: 4, 1 Class I2025: 32026 (partial year): 4
2007high 9 (2019) · low 0 (2008)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · DPS

55in 2025

2007: 92008: 172009: 142010: 212011: 1212012: 562013: 152014: 152015: 302016: 122017: 152018: 192019: 272020: 592021: 242022: 592023: 542024: 642025: 55
2007high 121 (2011) · low 9 (2007)2025

MAUDE reports naming product code DPS, 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
2007118729
20081331017
20091484114
201011104221
2011221541121
201212117056
201310134015
201411253015
20158178030
201611229012
20179177015
201814221019
20193178927
20206224259
20215135124
20226244159
202310236354
202482604 (1)64
20256163355
202662584—

More from Mortara Instrument, Inc.

51 FDA decisions under this applicant name. See the company

  • K182297Surveyor S2Mortara Instrument, Inc. · 2019
  • K173765Surveyor Patient MonitorMortara Instrument, Inc. · 20182 recalls
  • K161517Mortara Surveyor Patient MonitorMortara Instrument, Inc. · 2017
  • K161465CardioConfirmMortara Instrument, Inc. · 2016
  • K160685Surveyor S4 Mobile MonitorMortara Instrument, Inc. · 20161 recall

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https://510kreport.com/device/K922927 · printed Nov 4, 2026

Cite this page

510(k) Report. “K922927: Mortara Instrument ST Central Station.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K922927

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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