Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K904261Substantially Equivalent

Litter, Nonridgid, Poleless, Nylon Stretcher

Dow Cover Co., Inc., New Haven CT / Traditional, Substantially Equivalent

K904261 is the FDA 510(k) clearance record for LITTER, NONRIDGID, POLELESS, NYLON STRETCHER, a class I device, cleared for Dow Cover Co., Inc. on under FDA product code FPP (Stretcher, Hand-Carried). FDA records list one 510(k) clearance for Dow Cover Co., Inc. As of , FDA records show no recalls naming K904261.

Clearance record

Decision date
Received
(28 days to decision)
Product code
FPP Stretcher, Hand-Carried
Regulation
21 CFR 880.6900
Device class
Class I
Review panel
General Hospital
Applicant
Dow Cover Co., Inc. 373 Lexington Ave., New Haven CT
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