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FDA 510(k)

DETACHATIP III PLUS INSTRUMENT TRAY MODEL 3-4343

K-Number: K123175 · 2013-02-21

ApplicantConmed Corporation
Decision Date2013-02-21
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DETACHATIP III PLUS INSTRUMENT TRAY MODEL 3-4343 is the device name listed in this FDA 510(k) record. The listed applicant is Conmed Corporation. It received FDA 510(k) clearance on 2013-02-21 under 510(k) number K123175. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DETACHATIP III PLUS INSTRUMENT TRAY MODEL 3-4343?

DETACHATIP III PLUS INSTRUMENT TRAY MODEL 3-4343 is a medical device that received FDA 510(k) clearance on 2013-02-21. The listed applicant is Conmed Corporation. The 510(k) number is K123175.

When did DETACHATIP III PLUS INSTRUMENT TRAY MODEL 3-4343 receive FDA 510(k) clearance?

DETACHATIP III PLUS INSTRUMENT TRAY MODEL 3-4343 received FDA 510(k) clearance on 2013-02-21, under 510(k) number K123175.

Who is the listed applicant for DETACHATIP III PLUS INSTRUMENT TRAY MODEL 3-4343?

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 PLUS INSTRUMENT TRAY MODEL 3-4343?

The FDA product code for DETACHATIP III PLUS INSTRUMENT TRAY MODEL 3-4343 is KCT.

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Related Devices (Code: KCT)

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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.

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