510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K003455Substantially Equivalent

Modification to Chad Therapeutics Oxymatic Model 401

Chad Therapeutics, Inc., Chatsworth CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K003455 is the FDA 510(k) clearance record for MODIFICATION TO CHAD THERAPEUTICS OXYMATIC MODEL 401, a class II device, cleared for Chad Therapeutics, Inc. on under FDA product code NFB (Conserver, Oxygen). FDA records list 17 510(k) clearances for Chad Therapeutics, Inc., from to . As of , FDA records show one recall naming K003455.

Clearance record

Decision date
Received
(29 days to decision)
Product code
NFB Conserver, Oxygen
Regulation
21 CFR 868.5905
Device class
Class II
Review panel
Anesthesiology
Applicant
Chad Therapeutics, Inc. 21622 Plummer St., Chatsworth CA
510(k) summary
Summary
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