510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K023420Substantially Equivalent

Pulsed Oxygen Conserving Device - Every Breath, Pocdeb, Reacteb

Medical Electronic Devices, Inc., Torrance CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K023420 is the FDA 510(k) clearance record for PULSED OXYGEN CONSERVING DEVICE - EVERY BREATH, POCDEB, REACTEB, a class II device, cleared for Medical Electronic Devices, Inc. on under FDA product code NFB (Conserver, Oxygen). FDA records list 7 510(k) clearances for Medical Electronic Devices, Inc., from to . As of , FDA records show no recalls naming K023420.

Clearance record

Decision date
Received
(14 days to decision)
Product code
NFB Conserver, Oxygen
Regulation
21 CFR 868.5905
Device class
Class II
Review panel
Anesthesiology
Applicant
Medical Electronic Devices, Inc. 2807 Oregon Ct. #D6, Torrance CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NFB

Trailing 12 months

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

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