510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K023014Substantially Equivalent

Vianox Delivery System, Model I

Pulmonox Medical, Inc., Edmonton, Ab, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K023014 is the FDA 510(k) clearance record for VIANOX DELIVERY SYSTEM, MODEL I, a class II device, cleared for Pulmonox Medical, Inc. on under FDA product code MRP (Analyzer, Nitric Oxide). FDA records list 3 510(k) clearances for Pulmonox Medical, Inc., from to . As of , FDA records show no recalls naming K023014.

Clearance record

Decision date
Received
(338 days to decision)
Product code
MRP Analyzer, Nitric Oxide
Regulation
21 CFR 868.2380
Device class
Class II
Review panel
Anesthesiology
Applicant
Pulmonox Medical, Inc. 10835-120th St., Edmonton, Ab, CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MRP

Trailing 12 months

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

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