510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K070120Substantially Equivalent

Autovent Model 4000

Allied Medical LLC, Saint Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K070120 is the FDA 510(k) clearance record for AUTOVENT MODEL 4000, a class II device, cleared for Allied Healthcare Products, Inc. on under FDA product code BTL (Ventilator, Emergency, Powered (Resuscitator)). FDA records list 26 510(k) clearances for Allied Medical LLC, from to . As of , FDA records show no recalls naming K070120.

Clearance record

Decision date
Received
(111 days to decision)
Product code
BTL Ventilator, Emergency, Powered (Resuscitator)
Regulation
21 CFR 868.5925
Device class
Class II
Review panel
Anesthesiology
Applicant
Allied Healthcare Products, Inc. 1720 Sublette Ave., Saint Louis MO
510(k) summary
Statement
Third party review
No

Clearances, product code BTL

Trailing 12 months

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

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