510(k) Report

510(k) · Cleared

Cleared

Besmed Peak Flow Meter

K172804510(k) TraditionalCleared Jan 11, 2018115-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

Besmed Health Business Corp · BZH Meter, Peak Flow, Spirometry

Cleared on Jan 11, 2018 as substantially equivalent to K781922 (Vitalograph, Ltd., 1979) after a 115-day review. Its family tree reaches back 1 generation to 1979.

Decided
Jan 11, 2018
Review
115 days
Class
Class II
Product code
BZH
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K781922 (1979). No later device cites it as a predicate yet.

K781922 · Pulmonary Monitor · Vitalograph, Ltd. · 19790
  1. Root · 1 generation backK781922 Pulmonary MonitorVitalograph, Ltd. · 1979
  2. This deviceK172804 Besmed Peak Flow MeterBesmed Health Business Corp · 2018
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K781922Pulmonary MonitorVitalograph, Ltd.1979—
0 (this device)K172804Besmed Peak Flow MeterBesmed Health Business Corp2018—
FIG. 1 — Lineage of K172804, 1979–2018Source: 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 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
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What was it cleared against? (1)

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
*K781922Pulmonary Monitor
Summary page 4
…BZH - Meter, Peak Flow, Spirometry Class II Predicate Device: Vitalograph Peak Flow Meter, K781922 Reference Device: MINI WRIGHT LR AFS, K952713 Device Description: The Besmed Peak Flow Meter is a hand…
Vitalograph, Ltd.1979—
†K952713Mini Wright LR AfsClement Clarke, Inc.1996—

Also cleared against K781922: 2 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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?

  • Its one ancestor has no recall.
  • 2 other devices also cite its predicate K781922.

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. 2018, this device’s year, is highlighted.

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—

What is it indicated for?

The intended device measures a patient's peak expiratory flow rate liters/minute.

Patient Population – Patients 5 years and older requiring the measurement of peak expiratory flow rate.

Environment – Anywhere a patient may require the measurement of peak expiratory flow.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K172804: Besmed Peak Flow Meter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K172804

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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