510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K922178Substantially Equivalent

Companion 318 Nasal CPAP System -- Modification

Medtronic, Inc., Lenexa KS / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K922178 is the FDA 510(k) clearance record for COMPANION 318 NASAL CPAP SYSTEM -- MODIFICATION, a class II device, cleared for Puritan Bennett Corp. on under FDA product code BYE (Attachment, Breathing, Positive End Expiratory Pressure). FDA records list 1,525 510(k) clearances for Medtronic, Inc., from to . As of , FDA records show no recalls naming K922178.

Clearance record

Decision date
Received
(21 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
Puritan Bennett Corp. 10800 Pflumm Rd., Lenexa KS
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 November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code BYE, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260