Weevac TC Hand Carried Rescue Stretcher

FDA 510(k) K910709 · W. Murphy Ent., Inc.

Substantially Equivalent

510(k) numberK910709

Submission

Device name
Weevac TC Hand Carried Rescue Stretcher
Applicant
W. Murphy Ent., Inc.
Ontario, CA
Received
February 20, 1991
Decision date
April 1, 1991
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
K902474Weevac 1 Portable Rescue StretcherFPP · Traditional 07/24/1990SE
K902521Weevac 6 Infant Evacuation StretcherFPP · Traditional 06/22/1990SE

Questions and answers

When was Weevac TC Hand Carried Rescue Stretcher cleared by the FDA?

Weevac TC Hand Carried Rescue Stretcher (K910709) received a 510(k) decision of Substantially Equivalent on April 1, 1991, 40 days after the submission was received.

What is the product code of K910709?

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