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FDA 510(k)

ANGIOTECH CVC

K-Number: K073520 · 2008-04-11

ApplicantAngiotech Pharmaceuticals, Inc.
Decision Date2008-04-11
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ANGIOTECH CVC is the device name listed in this FDA 510(k) record. The listed applicant is Angiotech Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 2008-04-11 under 510(k) number K073520. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIOTECH CVC?

ANGIOTECH CVC is a medical device that received FDA 510(k) clearance on 2008-04-11. The listed applicant is Angiotech Pharmaceuticals, Inc.. The 510(k) number is K073520.

When did ANGIOTECH CVC receive FDA 510(k) clearance?

ANGIOTECH CVC received FDA 510(k) clearance on 2008-04-11, under 510(k) number K073520.

Who is the listed applicant for ANGIOTECH CVC?

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

What is the FDA product code for ANGIOTECH CVC?

The FDA product code for ANGIOTECH CVC is FOZ.

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Related Devices (Code: FOZ)

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Official Source

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

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