FDA 510(k)

SKINTACT COOL CONTACT ELECTROSURGICAL GROUNDING PLATES

K-Number: K030362 · 2003-04-14

Decision Date2003-04-14

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SKINTACT COOL CONTACT ELECTROSURGICAL GROUNDING PLATES is the device name listed in this FDA 510(k) record. The listed applicant is Leonhard Lang GmbH. It received FDA 510(k) clearance on 2003-04-14 under 510(k) number K030362. 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 SKINTACT COOL CONTACT ELECTROSURGICAL GROUNDING PLATES?

SKINTACT COOL CONTACT ELECTROSURGICAL GROUNDING PLATES is a medical device that received FDA 510(k) clearance on 2003-04-14. The listed applicant is Leonhard Lang GmbH. The 510(k) number is K030362.

When did SKINTACT COOL CONTACT ELECTROSURGICAL GROUNDING PLATES receive FDA 510(k) clearance?

SKINTACT COOL CONTACT ELECTROSURGICAL GROUNDING PLATES received FDA 510(k) clearance on 2003-04-14, under 510(k) number K030362.

Who is the listed applicant for SKINTACT COOL CONTACT ELECTROSURGICAL GROUNDING PLATES?

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

What is the FDA product code for SKINTACT COOL CONTACT ELECTROSURGICAL GROUNDING PLATES?

The FDA product code for SKINTACT COOL CONTACT ELECTROSURGICAL GROUNDING PLATES is GEI.

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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.