510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K000653Substantially Equivalent

Aeronox Universal, Model P/n 360000, Aeronox Bedside, Model P/n 360001, Aeronox Transport Transport, Model P/n 360002

Pulmonox Medical, Inc., Tofield, Alberta, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K000653 is the FDA 510(k) clearance record for AERONOX UNIVERSAL, MODEL P/N 360000, AERONOX BEDSIDE, MODEL P/N 360001, AERONOX TRANSPORT TRANSPORT, MODEL P/N 360002, a class II device, cleared for Pulmonox Medical Corp. on under FDA product code MRN (Apparatus, Nitric Oxide Delivery). FDA records list 3 510(k) clearances for Pulmonox Medical Corp., from to . As of , FDA records show no recalls naming K000653.

Clearance record

Decision date
Received
(158 days to decision)
Product code
MRN Apparatus, Nitric Oxide Delivery
Regulation
21 CFR 868.5165
Device class
Class II
Review panel
Anesthesiology
Applicant
Pulmonox Medical Corp. 5243-53 Ave., Tofield, Alberta, CA
510(k) summary
Summary
Third party review
No

Clearances, product code MRN

Trailing 12 months

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

FDA records show no clearances under product code MRN in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MRN, 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