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
K760680Substantially Equivalent

Intermittent Mandatory Ventilation

B & F Medical Products, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K760680 is the FDA 510(k) clearance record for INTERMITTENT MANDATORY VENTILATION, a class II device, cleared for B & F Medical Products, Inc. on under FDA product code CBO (Attachment, Intermittent Mandatory Ventilation (Imv)). FDA records list 18 510(k) clearances for B & F Medical Products, Inc., from to . As of , FDA records show no recalls naming K760680.

Clearance record

Decision date
Received
(7 days to decision)
Product code
CBO Attachment, Intermittent Mandatory Ventilation (Imv)
Regulation
21 CFR 868.5955
Device class
Class II
Review panel
Anesthesiology
Applicant
B & F Medical Products, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code CBO

Trailing 12 months

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

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