510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K840796Substantially Equivalent

Tender Lifting Care

Lancer Assoc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K840796 is the FDA 510(k) clearance record for TENDER LIFTING CARE, a class II device, cleared for Lancer Assoc. on under FDA product code FRZ (Device, Patient Transfer, Powered). FDA records list 2 510(k) clearances for Lancer Assoc., from to . As of , FDA records show no recalls naming K840796.

Clearance record

Decision date
Received
(57 days to decision)
Product code
FRZ Device, Patient Transfer, Powered
Regulation
21 CFR 880.6775
Device class
Class II
Review panel
General Hospital
Applicant
Lancer Assoc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code FRZ

Trailing 12 months

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

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