FDA 510(k)

HANCOCK AORTIC PUNCH

K-Number: K800122 · 1980-02-01

Decision Date1980-02-01

Product CodeDWS

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

HANCOCK AORTIC PUNCH is the device name listed in this FDA 510(k) record. The listed applicant is Hancock Laboratories, Inc.. It received FDA 510(k) clearance on 1980-02-01 under 510(k) number K800122. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HANCOCK AORTIC PUNCH?

HANCOCK AORTIC PUNCH is a medical device that received FDA 510(k) clearance on 1980-02-01. The listed applicant is Hancock Laboratories, Inc.. The 510(k) number is K800122.

When did HANCOCK AORTIC PUNCH receive FDA 510(k) clearance?

HANCOCK AORTIC PUNCH received FDA 510(k) clearance on 1980-02-01, under 510(k) number K800122.

Who is the listed applicant for HANCOCK AORTIC PUNCH?

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

What is the FDA product code for HANCOCK AORTIC PUNCH?

The FDA product code for HANCOCK AORTIC PUNCH is DWS.

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Other records listing Hancock Laboratories, Inc. as applicant

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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.