FDA 510(k)

DETACHATIP III

K-Number: K123260 · 2012-12-21

Decision Date2012-12-21

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

DETACHATIP III is the device name listed in this FDA 510(k) record. The listed applicant is Conmed Corporation. It received FDA 510(k) clearance on 2012-12-21 under 510(k) number K123260. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DETACHATIP III?

DETACHATIP III is a medical device that received FDA 510(k) clearance on 2012-12-21. The listed applicant is Conmed Corporation. The 510(k) number is K123260.

When did DETACHATIP III receive FDA 510(k) clearance?

DETACHATIP III received FDA 510(k) clearance on 2012-12-21, under 510(k) number K123260.

Who is the listed applicant for DETACHATIP III?

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 DETACHATIP III?

The FDA product code for DETACHATIP III is GEI.

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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.