510(k) Report

510(k) · Cleared

Cleared

Airwatch Monitor

K941226510(k) TraditionalCleared Nov 16, 1994247-day reviewClass II21 CFR 868.1860

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

Enact Health Management Systems · BZH Meter, Peak Flow, Spirometry

Cleared on Nov 16, 1994 after a 247-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 2 later devices descend from it.

Decided
Nov 16, 1994
Review
247 days
Class
Class II
Product code
BZH
Recalls
None
Predicates
0

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

Descendants, by year cleared 1998: 2 descendants cleared1990200020102020
  1. This deviceK941226 Airwatch MonitorEnact Health Management Systems · 1994
  2. Descendant · cites it directly · 0 of its ownK982675 Airwatch II ZonelessEnact Health Management Systems · 1998
  3. Descendant · cites it directly · 0 of its ownK982676 Airwatch II ZoneEnact Health Management Systems · 1998

Most influential descendants

Showing 2 of 2 · See all
  • K982675Airwatch II ZonelessEnact Health Management Systems · 1998 · cites it directly0descendants
  • K982676Airwatch II ZoneEnact Health Management Systems · 1998 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K941226Airwatch MonitorEnact Health Management Systems1994—
+1K982675Airwatch II ZonelessEnact Health Management Systems1998—
+1K982676Airwatch II ZoneEnact Health Management Systems1998—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199820
FIG. 1 — Lineage of K941226, 1994–1998Source: 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 BZH? 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 BZH device

  1. #1 K252802 Peak Flow Meter (PF-10(BR-PEF231))score 13.5 · 8 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? (2)

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

NumberDeviceApplicantDecidedDescendants
K982675Airwatch II ZonelessEnact Health Management Systems19980
K982676Airwatch II ZoneEnact Health Management Systems19980

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, K982675 (Enact Health Management Systems, 1998) has gone furthest, with 0 descendants of its own.

How does its category compare?

All BZH devices

BZH Meter, Peak Flow, Spirometry: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · BZH

3in 2024

2009: 22010: 22013: 12014: 12016: 12017: 12018: 32019: 12020: 22021: 12023: 12024: 32026 (partial year): 2
2007high 3 (2018) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · BZH

371in 2024

2018: 115 days median2024: 371 days median
2007high 371 (2024) · low 115 (2018)2026

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

Recalls per year · BZH

No recall names BZH since 2007.

Adverse event reports per year · BZH

1in 2015

2007: 12011: 12013: 32014: 222015: 1
2007high 22 (2014) · low 0 (2008)2025

MAUDE reports naming product code BZH, 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
20070—01
20080—00
20092—00
20102—00
20110—01
20120—00
20131—03
20141—022
20150—01
20161—00
20171—00
2018311500
20191—00
20202—00
20211—00
20220—00
20231—00
2024337100
20250—00
20262—0—
Cite this page

510(k) Report. “K941226: Airwatch Monitor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K941226

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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