510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K952713Substantially Equivalent

Mini Wright Lr Afs

Clement Clarke, Inc., England, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K952713 is the FDA 510(k) clearance record for MINI WRIGHT LR AFS, a class II device, cleared for Clement Clarke, Inc. on under FDA product code BZH (Meter, Peak Flow, Spirometry). FDA records list 10 510(k) clearances for Clement Clarke, Inc., from to . As of , FDA records show no recalls naming K952713.

Clearance record

Decision date
Received
(289 days to decision)
Product code
BZH Meter, Peak Flow, Spirometry
Regulation
21 CFR 868.1860
Device class
Class II
Review panel
Anesthesiology
Applicant
Clement Clarke, Inc. Airmed House, Edinburgh Way, England, GB
510(k) summary
Statement
Third party review
No

Clearances, product code BZH

Trailing 12 months
2 clearances under product code BZH in the twelve months to October 2026, May 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code BZH, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20261
July 20260
August 20260
September 20260
October 20260