510(k) Report

510(k) · Cleared

Cleared

Model 2000W Option H Configuration

K871302510(k) TraditionalCleared Apr 20, 198719-day reviewClass II21 CFR 868.2375

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

Edentec Corp. · BZQ Monitor, Breathing Frequency

Cleared on Apr 20, 1987 after a 19-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 later devices descend from it.

Decided
Apr 20, 1987
Review
19 days
Class
Class II
Product code
BZQ
Recalls
None
Predicates
0

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

Descendants, by year cleared 2000: 1 descendant cleared1997: 1 descendant cleared1990200020102020
  1. This deviceK871302 Model 2000W Option H ConfigurationEdentec Corp. · 1987
  2. Descendant · cites it directly · 0 of its ownK991087 Hannah Wireless Vital Signs MonitorIlife Systems, Inc. · 2000
  3. Descendant · cites it directly · 0 of its ownK962781 Corometrics Model 510 and 511 MonitorGe Medical Systems Information Technologies · 1997 · Recalled

Most influential descendants

Showing 2 of 2 · See all
  • K991087Hannah Wireless Vital Signs MonitorIlife Systems, Inc. · 2000 · cites it directly0descendants
  • K962781Corometrics Model 510 and 511 MonitorGe Medical Systems Information Technologies · 1997 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K871302Model 2000W Option H ConfigurationEdentec Corp.1987—
+1K991087Hannah Wireless Vital Signs MonitorIlife Systems, Inc.2000—
+1K962781Corometrics Model 510 and 511 MonitorGe Medical Systems Information Technologies19971

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199710
200010
FIG. 1 — Lineage of K871302, 1987–2000Source: 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 BZQ? 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 BZQ device

  1. #1 K251326 Respiration Rate algorithmscore 20.2 · 30 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? (2)

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

NumberDeviceApplicantDecidedDescendants
K991087Hannah Wireless Vital Signs MonitorIlife Systems, Inc.20000
K962781Corometrics Model 510 and 511 MonitorGe Medical Systems Information Technologies19970

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, K991087 (Ilife Systems, Inc., 2000) has gone furthest, with 0 descendants of its own.

How does its category compare?

All BZQ devices

BZQ Monitor, Breathing Frequency: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · BZQ

7in 2025

2007: 22008: 12009: 32010: 22011: 12012: 22013: 32014: 22016: 22018: 32019: 12020: 22021: 22022: 32023: 12024: 12025: 72026 (partial year): 2
2007high 7 (2025) · low 0 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · BZQ

255in 2025

2009: 121 days median2013: 261 days median2018: 198 days median2022: 198 days median2025: 255 days median
2007high 261 (2013) · low 121 (2009)2026

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

Recalls per year · BZQ

1in 2010

2010: 1
2007high 1 (2010) · low 0 (2007)2026

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

Adverse event reports per year · BZQ

2in 2022

2007: 72009: 12010: 12012: 32017: 112018: 102019: 132020: 102021: 12022: 2
2007high 13 (2019) · low 0 (2008)2025

MAUDE reports naming product code BZQ, 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
20072—07
20081—00
2009312101
20102—11
20111—00
20122—03
2013326100
20142—00
20150—00
20162—00
20170—011
20183198010
20191—013
20202—010
20212—01
2022319802
20231—00
20241—00
2025725500
20262—0—
Cite this page

510(k) Report. “K871302: Model 2000W Option H Configuration.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K871302

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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