Anchor Tissue Retrieval System by CONMED
K-Number: K173822 · 2018-09-11
Device Summary
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. The listed applicant is Conmed Corporation. The 510(k) number is K173822.
When did Anchor Tissue Retrieval System by CONMED receive FDA 510(k) clearance?
Anchor Tissue Retrieval System by CONMED received FDA 510(k) clearance on 2018-09-11, under 510(k) number K173822.
Who is the listed applicant for Anchor Tissue Retrieval System by CONMED?
The FDA 510(k) record lists Conmed Corporation as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Conmed Corporation as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: GCJ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.