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FDA 510(k)

TROKAMED GMBH ELECTROSURGICAL INSTRUMENTS & ACCESSORIES

K-Number: K060232 · 2006-07-12

ApplicantTrokamed GmbH
Decision Date2006-07-12
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TROKAMED GMBH ELECTROSURGICAL INSTRUMENTS & ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Trokamed GmbH. It received FDA 510(k) clearance on 2006-07-12 under 510(k) number K060232. 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 TROKAMED GMBH ELECTROSURGICAL INSTRUMENTS & ACCESSORIES?

TROKAMED GMBH ELECTROSURGICAL INSTRUMENTS & ACCESSORIES is a medical device that received FDA 510(k) clearance on 2006-07-12. The listed applicant is Trokamed GmbH. The 510(k) number is K060232.

When did TROKAMED GMBH ELECTROSURGICAL INSTRUMENTS & ACCESSORIES receive FDA 510(k) clearance?

TROKAMED GMBH ELECTROSURGICAL INSTRUMENTS & ACCESSORIES received FDA 510(k) clearance on 2006-07-12, under 510(k) number K060232.

Who is the listed applicant for TROKAMED GMBH ELECTROSURGICAL INSTRUMENTS & ACCESSORIES?

The FDA 510(k) record lists Trokamed GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TROKAMED GMBH ELECTROSURGICAL INSTRUMENTS & ACCESSORIES?

The FDA product code for TROKAMED GMBH ELECTROSURGICAL INSTRUMENTS & ACCESSORIES is GEI.

Related Clinical Trials

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Other records listing Trokamed GmbH 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.

K200770Mini PCNL-SystemK091010TROKAMED MORCELLATORK060233TROKAMED GMBH ENDOSCOPES AND ACCESSORIES

Related Devices (Code: GEI)

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.

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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.

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