FDA 510(k)

ANGIOMAT CT INJECTOR

K-Number: K873687 · 1987-10-09

Decision Date1987-10-09

Product CodeDXT

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

ANGIOMAT CT INJECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Mallinckrodt Group, Inc.. It received FDA 510(k) clearance on 1987-10-09 under 510(k) number K873687. 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 ANGIOMAT CT INJECTOR?

ANGIOMAT CT INJECTOR is a medical device that received FDA 510(k) clearance on 1987-10-09. The listed applicant is Mallinckrodt Group, Inc.. The 510(k) number is K873687.

When did ANGIOMAT CT INJECTOR receive FDA 510(k) clearance?

ANGIOMAT CT INJECTOR received FDA 510(k) clearance on 1987-10-09, under 510(k) number K873687.

Who is the listed applicant for ANGIOMAT CT INJECTOR?

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

What is the FDA product code for ANGIOMAT CT INJECTOR?

The FDA product code for ANGIOMAT CT INJECTOR is DXT.

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Other records listing Mallinckrodt Group, Inc. as applicant

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Related Devices (Code: DXT)

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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.