510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K974254Substantially Equivalent

Benefit B3--- Series

M.C. Healthcare Products, Inc., Beamsville, Ontario, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K974254 is the FDA 510(k) clearance record for BENEFIT B3--- SERIES, a class II device, cleared for M.C. Healthcare Products, Inc. on under FDA product code FNL (Bed, Ac-Powered Adjustable Hospital). FDA records list 2 510(k) clearances for M.C. Healthcare Products, Inc., from to . As of , FDA records show no recalls naming K974254.

Clearance record

Decision date
Received
(33 days to decision)
Product code
FNL Bed, Ac-Powered Adjustable Hospital
Regulation
21 CFR 880.5100
Device class
Class II
Review panel
General Hospital
Applicant
M.C. Healthcare Products, Inc. 4658 Ontario St., Beamsville, Ontario, CA
510(k) summary
Statement
Third party review
No

Clearances, product code FNL

Trailing 12 months

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

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