510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K955047Substantially Equivalent

Westmed Circularie Pep Devices

Westmed Intl., Tucson AZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K955047 is the FDA 510(k) clearance record for WESTMED CIRCULARIE PEP DEVICES, a class II device, cleared for Westmed Intl. on under FDA product code BYE (Attachment, Breathing, Positive End Expiratory Pressure). FDA records list 9 510(k) clearances for Westmed Intl., from to . As of , FDA records show no recalls naming K955047.

Clearance record

Decision date
Received
(145 days to decision)
Product code
BYE Attachment, Breathing, Positive End Expiratory Pressure
Regulation
21 CFR 868.5965
Device class
Class II
Review panel
Anesthesiology
Applicant
Westmed Intl. 3351 E. Hemisphere Loop, Tucson AZ
510(k) summary
Statement
Third party review
No

Clearances, product code BYE

Trailing 12 months

FDA records hold no clearances under product code BYE in the trailing twelve months.

FDA records show no clearances under product code BYE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code BYE, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260