510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K833327Substantially Equivalent

Respironics Pr Valve

Respironics, Inc., Monroeville PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K833327 is the FDA 510(k) clearance record for RESPIRONICS PR VALVE, a class II device, cleared for Respironics, Inc. on under FDA product code BSK (Cuff, Tracheal Tube, Inflatable). FDA records list 186 510(k) clearances for Respironics, Inc., from to . As of , FDA records show no recalls naming K833327.

Clearance record

Decision date
Received
(62 days to decision)
Product code
BSK Cuff, Tracheal Tube, Inflatable
Regulation
21 CFR 868.5750
Device class
Class II
Review panel
Anesthesiology
Applicant
Respironics, Inc. 530 Seco Rd., Monroeville PA
Third party review
No

Clearances, product code BSK

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