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FDA 510(k)

MEDRAD CONTRAST HOLDER

K-Number: K964782 · 1997-02-25

ApplicantMedrad, Inc.
Decision Date1997-02-25
Product CodeFOX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDRAD CONTRAST HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Medrad, Inc.. It received FDA 510(k) clearance on 1997-02-25 under 510(k) number K964782. The device is classified under product code FOX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDRAD CONTRAST HOLDER?

MEDRAD CONTRAST HOLDER is a medical device that received FDA 510(k) clearance on 1997-02-25. The listed applicant is Medrad, Inc.. The 510(k) number is K964782.

When did MEDRAD CONTRAST HOLDER receive FDA 510(k) clearance?

MEDRAD CONTRAST HOLDER received FDA 510(k) clearance on 1997-02-25, under 510(k) number K964782.

Who is the listed applicant for MEDRAD CONTRAST HOLDER?

The FDA 510(k) record lists Medrad, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDRAD CONTRAST HOLDER?

The FDA product code for MEDRAD CONTRAST HOLDER is FOX.

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Other records listing Medrad, Inc. as applicant

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Related Devices (Code: FOX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K980336IV STANDSClinton Industries, Inc.K961470PORT-A-POLEPrins Medical Ind., Inc.K960027HIGH VOLUME I.V. & IRRIGATION TOWERAllen Medical Systems, Inc.K952196IV POLE/STANDValentine Intl. , Ltd.K950367IV SHUTTLEEquipment Concepts, Inc.K946201STAND, INFUSIONMedical Specialties, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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