Hand-Carried Stretchers

FDA 510(k) K904494 · Minto Research & Development, Inc.

Substantially Equivalent

510(k) numberK904494

Submission

Device name
Hand-Carried Stretchers
Applicant
Minto Research & Development, Inc.
Redding, CA, US
Received
October 2, 1990
Decision date
October 12, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FPP – Stretcher, Hand-Carried
Device class
Class I (low risk)
Regulation
21 CFR 880.6900
Specialty
General Hospital

Other 510(k)s with product code FPP

510(k)DeviceApplicantDecision
K030283Baby PodFPP · Traditional Prism Enterprises, Inc.04/22/2003SE
K942356MED-EVAC-4 Medical Evacuation StretcherFPP · Traditional Montery Bay Corp.07/19/1994SE
K940130Stryker Model 6110 Emergency/Pole StretcherFPP · Traditional Stryker Corp.03/10/1994SE
K940245Evacu-SledFPP · Traditional Evacu Technologies, Inc.02/28/1994SE
K924275Restraining StretcherFPP · Traditional Dms07/27/1993SE
K922816U P Custom Design, Inc. Cot Equipment CarrierFPP · Traditional Up Custom Design, Inc.07/13/1993SE
K924669Ferno-Washington Basket Stretcher, Model 71-WFPP · Traditional Ferno04/29/1993SE
K920805Life Lite Emergency StretcherFPP · Traditional Design Principles, Inc.05/22/1992SE
K915874Basket Litter CarrierFPP · Traditional Bradco Med , Ltd.05/13/1992SE
K914140Grassi Gastrojejun Tube Gastric Decomp/Jejun FeedFPP · Traditional Bissell Medical Products, Inc.03/31/1992SE

More from Bissell Medical Products, Inc.

510(k)DeviceDecision
K940590Minto Skin Traction MotorITH · Traditional 04/15/1994SE
K904723ForcepsGEN · Traditional 07/26/1991SE
K904511Hand-Carried Stretchers/Break Away FlatFPP · Traditional 10/12/1990SE

Questions and answers

When was Hand-Carried Stretchers cleared by the FDA?

Hand-Carried Stretchers (K904494) received a 510(k) decision of Substantially Equivalent on October 12, 1990, 10 days after the submission was received.

What is the product code of K904494?

The FDA product code is FPP – Stretcher, Hand-Carried, a Class I (low risk) device regulated under 21 CFR 880.6900.