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FDA 510(k)

MEDRAD MCT, MCT PLUS INJECTOR/MEDRAD FRONT LOAD

K-Number: K924116 · 1993-01-21

ApplicantMedrad, Inc.
Decision Date1993-01-21
Product CodeDXT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDRAD MCT, MCT PLUS INJECTOR/MEDRAD FRONT LOAD is the device name listed in this FDA 510(k) record. The listed applicant is Medrad, Inc.. It received FDA 510(k) clearance on 1993-01-21 under 510(k) number K924116. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDRAD MCT, MCT PLUS INJECTOR/MEDRAD FRONT LOAD?

MEDRAD MCT, MCT PLUS INJECTOR/MEDRAD FRONT LOAD is a medical device that received FDA 510(k) clearance on 1993-01-21. The listed applicant is Medrad, Inc.. The 510(k) number is K924116.

When did MEDRAD MCT, MCT PLUS INJECTOR/MEDRAD FRONT LOAD receive FDA 510(k) clearance?

MEDRAD MCT, MCT PLUS INJECTOR/MEDRAD FRONT LOAD received FDA 510(k) clearance on 1993-01-21, under 510(k) number K924116.

Who is the listed applicant for MEDRAD MCT, MCT PLUS INJECTOR/MEDRAD FRONT LOAD?

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 MCT, MCT PLUS INJECTOR/MEDRAD FRONT LOAD?

The FDA product code for MEDRAD MCT, MCT PLUS INJECTOR/MEDRAD FRONT LOAD is DXT.

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Related Devices (Code: DXT)

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.

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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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