FDA 510(k)

CORLINK AUTOMATED ANASTOMOTIC SYSTEM

K-Number: K033979 · 2004-03-31

Decision Date2004-03-31

Product CodeFZP

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

CORLINK AUTOMATED ANASTOMOTIC SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is By-Pass Makafim , Ltd.. It received FDA 510(k) clearance on 2004-03-31 under 510(k) number K033979. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORLINK AUTOMATED ANASTOMOTIC SYSTEM?

CORLINK AUTOMATED ANASTOMOTIC SYSTEM is a medical device that received FDA 510(k) clearance on 2004-03-31. The listed applicant is By-Pass Makafim , Ltd.. The 510(k) number is K033979.

When did CORLINK AUTOMATED ANASTOMOTIC SYSTEM receive FDA 510(k) clearance?

CORLINK AUTOMATED ANASTOMOTIC SYSTEM received FDA 510(k) clearance on 2004-03-31, under 510(k) number K033979.

Who is the listed applicant for CORLINK AUTOMATED ANASTOMOTIC SYSTEM?

The FDA 510(k) record lists By-Pass Makafim , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORLINK AUTOMATED ANASTOMOTIC SYSTEM?

The FDA product code for CORLINK AUTOMATED ANASTOMOTIC SYSTEM is FZP.

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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.