General Procedural Stretchers (P880- P886)

FDA 510(k) K922809 · Hill-Rom, Inc.

Substantially Equivalent

510(k) numberK922809

Submission

Device name
General Procedural Stretchers (P880- P886)
Applicant
Hill-Rom, Inc.
Batesville, TN, US
Received
June 10, 1992
Decision date
March 31, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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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Questions and answers

When was General Procedural Stretchers (P880- P886) cleared by the FDA?

General Procedural Stretchers (P880- P886) (K922809) received a 510(k) decision of Substantially Equivalent on March 31, 1993, 294 days after the submission was received.

What is the product code of K922809?

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