510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K920704Substantially Equivalent

Stryker i.v. Caddy Accessory Device

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

K920704 is the FDA 510(k) clearance record for STRYKER I.V. CADDY ACCESSORY DEVICE, a class II device, cleared for Stryker Medical on under FDA product code FPO (Stretcher, Wheeled). FDA records list 14 510(k) clearances for Stryker Medical, from to . As of , FDA records show no recalls naming K920704.

Clearance record

Decision date
Received
(34 days to decision)
Product code
FPO Stretcher, Wheeled
Regulation
21 CFR 880.6910
Device class
Class II
Review panel
General Hospital
Applicant
Stryker Medical 6300 S. Sprinkle Rd., 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 October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FPO, 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