FDA 510(k)

ANGIOMAT 6000

K-Number: K860204 · 1986-05-02

Decision Date1986-05-02

Product CodeDXT

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

ANGIOMAT 6000 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 1986-05-02 under 510(k) number K860204. 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 6000?

ANGIOMAT 6000 is a medical device that received FDA 510(k) clearance on 1986-05-02. The listed applicant is Mallinckrodt Group, Inc.. The 510(k) number is K860204.

When did ANGIOMAT 6000 receive FDA 510(k) clearance?

ANGIOMAT 6000 received FDA 510(k) clearance on 1986-05-02, under 510(k) number K860204.

Who is the listed applicant for ANGIOMAT 6000?

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 6000?

The FDA product code for ANGIOMAT 6000 is 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.