Anchor Tissue Retrieval System by CONMED
K-Number: K173822 · 2018-09-11
ApplicantConmed Corporation
Decision Date2018-09-11
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Anchor Tissue Retrieval System by CONMED is a medical device manufactured by Conmed Corporation. It received FDA 510(k) clearance on 2018-09-11 under approval number K173822. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Anchor Tissue Retrieval System by CONMED?
Anchor Tissue Retrieval System by CONMED is a medical device that received FDA 510(k) clearance on 2018-09-11. It is manufactured by Conmed Corporation. The 510(k) number is K173822.
When was Anchor Tissue Retrieval System by CONMED approved by the FDA?
Anchor Tissue Retrieval System by CONMED received FDA 510(k) clearance on 2018-09-11, under approval number K173822.
What company makes Anchor Tissue Retrieval System by CONMED?
Anchor Tissue Retrieval System by CONMED is manufactured by Conmed Corporation.
What is the FDA product code for Anchor Tissue Retrieval System by CONMED?
The FDA product code for Anchor Tissue Retrieval System by CONMED is GCJ.
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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.