510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K924272Substantially Equivalent

Mediresp III

Medflow Corp., Inc., Hilton NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K924272 is the FDA 510(k) clearance record for MEDIRESP III, a class II device, cleared for Medflow Corp., Inc. on under FDA product code BTL (Ventilator, Emergency, Powered (Resuscitator)). FDA records list one 510(k) clearance for Medflow Corp., Inc. As of , FDA records show no recalls naming K924272.

Clearance record

Decision date
Received
(534 days to decision)
Product code
BTL Ventilator, Emergency, Powered (Resuscitator)
Regulation
21 CFR 868.5925
Device class
Class II
Review panel
Anesthesiology
Applicant
Medflow Corp., Inc. 100 Hogan Pt. Rd., Hilton NY
510(k) summary
Summary
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