Hare Model 2000 Ez Loader Model 95555

FDA 510(k) K962181 · Dyna Corp.

Substantially Equivalent

510(k) numberK962181

Submission

Device name
Hare Model 2000 Ez Loader Model 95555
Applicant
Dyna Corp.
Carlsbad, CA, US
Received
June 6, 1996
Decision date
August 1, 1996
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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Questions and answers

When was Hare Model 2000 Ez Loader Model 95555 cleared by the FDA?

Hare Model 2000 Ez Loader Model 95555 (K962181) received a 510(k) decision of Substantially Equivalent on August 1, 1996, 56 days after the submission was received.

What is the product code of K962181?

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