510(k) Report

510(k) · Cleared

Cleared

Electronic Peak Flow Meter

K230423510(k) TraditionalCleared Feb 23, 2024371-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

Taian Dalu Medical Instrument Co., Ltd. · BZH Meter, Peak Flow, Spirometry

Cleared on Feb 23, 2024 as substantially equivalent to K170281 (Beijing M&B Electronic Instruments Co., Ltd., 2017) after a 371-day review. Its family tree reaches back 2 generations to 2014.

Decided
Feb 23, 2024
Review
371 days
Class
Class II
Product code
BZH
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K133975 (2014). No later device cites it as a predicate yet.

  1. Root · 2 generations backK133975 MSA100 Peak Flow MeterBeijing M&B Electronic Instruments Co., Ltd. · 2014
  2. 1 generation backK170281 MSA100BT Peak Flow MeterBeijing M&B Electronic Instruments Co., Ltd. · 2017
  3. This deviceK230423 Electronic Peak Flow MeterTaian Dalu Medical Instrument Co., Ltd. · 2024
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K133975MSA100 Peak Flow MeterBeijing M&B Electronic Instruments Co., Ltd.2014—
−1K170281MSA100BT Peak Flow MeterBeijing M&B Electronic Instruments Co., Ltd.2017—
0 (this device)K230423Electronic Peak Flow MeterTaian Dalu Medical Instrument Co., Ltd.2024—
FIG. 1 — Lineage of K230423, 2014–2024Source: 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), 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
*K170281MSA100BT Peak Flow Meter
Summary page 5
…Regulation No. 21 CFR 868.1860 3. Legally Marketed Predicate Device Trade Name MSA100BT Peak Flow Meter 510(k) Number K170281 Product Code BZH Manufacturer Beijing M&B Electronic Instruments Co., Ltd.…
Beijing M&B Electronic Instruments Co., Ltd.2017—

Also cleared against K170281: 1 other device →

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?

  • The line of descent spans 10 years and passes through 2 companies; a new generation was cleared every 6.4 years on median.
  • None of the 2 ancestors has a recall.
  • 1 other device also cites its predicate K170281.

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. 2024, 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?

This device is intended for monitoring PEF (Peak Expiratory Flow) for patient home use. The device is designed for children 5 years of age or older, adolescent and adult subjects.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K230423: Electronic Peak Flow Meter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K230423

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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