Medrad Contrast Holder

FDA 510(k) K964782 · Medrad, Inc.

Substantially Equivalent

510(k) numberK964782

Submission

Device name
Medrad Contrast Holder
Applicant
Medrad, Inc.
Indianola, PA, US
Received
November 27, 1996
Decision date
February 25, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FOX – Stand, Infusion
Device class
Class I (low risk)
Regulation
21 CFR 880.6990
Specialty
General Hospital

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K952196IV Pole/StandFOX · Traditional Valentine Intl. , Ltd.07/31/1995SE
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K946201Stand, InfusionFOX · Traditional Medical Specialties, Inc.04/18/1995SE
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K932498Mobile Care IV StandFOX · Traditional Mobile Care, Inc.10/27/1993SE
K925066Pneumatic Irrigation StandardFOX · Traditional Arthrodyn, Inc.07/28/1993SE
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Questions and answers

When was Medrad Contrast Holder cleared by the FDA?

Medrad Contrast Holder (K964782) received a 510(k) decision of Substantially Equivalent on February 25, 1997, 90 days after the submission was received.

What is the product code of K964782?

The FDA product code is FOX – Stand, Infusion, a Class I (low risk) device regulated under 21 CFR 880.6990.