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
K940130Substantially Equivalent

Stryker Model 6110 Emergency/pole Stretcher

Stryker Corp., Kalamazoo MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K940130 is the FDA 510(k) clearance record for STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER, a class I device, cleared for Stryker Corp. on under FDA product code FPP (Stretcher, Hand-Carried). FDA records list 568 510(k) clearances for Stryker Corp., from to . As of , FDA records show no recalls naming K940130.

Clearance record

Decision date
Received
(66 days to decision)
Product code
FPP Stretcher, Hand-Carried
Regulation
21 CFR 880.6900
Device class
Class I
Review panel
General Hospital
Applicant
Stryker Corp. Medical Div., Kalamazoo MI
510(k) summary
Statement
Third party review
No

Clearances, product code FPP

Trailing 12 months

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

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