510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K895677Substantially Equivalent

The Murray Mobilift(tm)

Medical/Surgical Specialties, Ltd., Kalamazoo MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K895677 is the FDA 510(k) clearance record for THE MURRAY MOBILIFT(TM), a class II device, cleared for Medical/Surgical Specialties, Ltd. on under FDA product code FNG (Lift, Patient, Ac-Powered). FDA records list 4 510(k) clearances for Medical/Surgical Specialties, Ltd., from to . As of , FDA records show no recalls naming K895677.

Clearance record

Decision date
Received
(401 days to decision)
Product code
FNG Lift, Patient, Ac-Powered
Regulation
21 CFR 880.5500
Device class
Class II
Review panel
General Hospital
Applicant
Medical/Surgical Specialties, Ltd. 1611 W. Centre St., Kalamazoo MI
Third party review
No

Clearances, product code FNG

Trailing 12 months

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

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