510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K072723Substantially Equivalent

Respironics Golox

Respironics, Inc., Murrysville PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K072723 is the FDA 510(k) clearance record for RESPIRONICS GOLOX, a class II device, cleared for Respironics, Inc. on under FDA product code BYJ (Unit, Liquid-Oxygen, Portable). FDA records list 186 510(k) clearances for Respironics, Inc., from to . As of , FDA records show no recalls naming K072723.

Clearance record

Decision date
Received
(176 days to decision)
Product code
BYJ Unit, Liquid-Oxygen, Portable
Regulation
21 CFR 868.5655
Device class
Class II
Review panel
Anesthesiology
Applicant
Respironics, Inc. 1740 Golden Mile Hwy., Murrysville PA
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code BYJ

Trailing 12 months

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

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