510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K853378Substantially Equivalent

Auto Pro

Respiration Technology, Inc., Denver CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K853378 is the FDA 510(k) clearance record for AUTO PRO, a class II device, cleared for Respiration Technology, Inc. on under FDA product code NFB (Conserver, Oxygen). FDA records list one 510(k) clearance for Respiration Technology, Inc. As of , FDA records show no recalls naming K853378.

Clearance record

Decision date
Received
(38 days to decision)
Product code
NFB Conserver, Oxygen
Regulation
21 CFR 868.5905
Device class
Class II
Review panel
Anesthesiology
Applicant
Respiration Technology, Inc. 4347 E. Colfax Ave., Denver CO
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