510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K942948Substantially Equivalent

Stryker Powered Stretcher

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

K942948 is the FDA 510(k) clearance record for STRYKER POWERED STRETCHER, a class II device, cleared for Stryker Corp. on under FDA product code FPO (Stretcher, Wheeled). FDA records list 568 510(k) clearances for Stryker Corp., from to . As of , FDA records show no recalls naming K942948.

Clearance record

Decision date
Received
(215 days to decision)
Product code
FPO Stretcher, Wheeled
Regulation
21 CFR 880.6910
Device class
Class II
Review panel
General Hospital
Applicant
Stryker Corp. Medical Div., Kalamazoo MI
510(k) summary
Statement
Third party review
No

Clearances, product code FPO

Trailing 12 months

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

FDA records show no clearances under product code FPO in the twelve months to November 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FPO, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260
November 20260