510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K930625Substantially Equivalent

Sanitas Patient Lift

Dutton-Lainson Co., Hastings NE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930625 is the FDA 510(k) clearance record for SANITAS PATIENT LIFT, a class I device, cleared for Dutton-Lainson Co. on under FDA product code FSA (Lift, Patient, Non-Ac-Powered). FDA records list 3 510(k) clearances for Dutton-Lainson Co., from to . As of , FDA records show no recalls naming K930625.

Clearance record

Decision date
Received
(217 days to decision)
Product code
FSA Lift, Patient, Non-Ac-Powered
Regulation
21 CFR 880.5510
Device class
Class I
Review panel
General Hospital
Applicant
Dutton-Lainson Co. 451 W. Second St., Hastings NE
510(k) summary
Statement
Third party review
No

Clearances, product code FSA

Trailing 12 months

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

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