Stryker Powered Stretcher

FDA 510(k) K942948 · Stryker Corp.

Substantially Equivalent

510(k) numberK942948

Submission

Device name
Stryker Powered Stretcher
Applicant
Stryker Corp.
Kalamazoo, MI, US
Received
June 23, 1994
Decision date
January 24, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
FPO – Stretcher, Wheeled
Device class
Class II (moderate risk)
Regulation
21 CFR 880.6910
Specialty
General Hospital

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K952447Hill-Rom Ambulatory Care Procedural StretcherFPO · Traditional Hill-Rom, Inc.11/22/1995SE
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Questions and answers

When was Stryker Powered Stretcher cleared by the FDA?

Stryker Powered Stretcher (K942948) received a 510(k) decision of Substantially Equivalent on January 24, 1995, 215 days after the submission was received.

What is the product code of K942948?

The FDA product code is FPO – Stretcher, Wheeled, a Class II (moderate risk) device regulated under 21 CFR 880.6910.