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FDA 510(k)

KLS MARTIN ELECTROSURGICAL INSTRUMENTS

K-Number: K082505 · 2009-06-12

ApplicantKl Martin L.P.
Decision Date2009-06-12
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KLS MARTIN ELECTROSURGICAL INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Kl Martin L.P.. It received FDA 510(k) clearance on 2009-06-12 under 510(k) number K082505. 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 KLS MARTIN ELECTROSURGICAL INSTRUMENTS?

KLS MARTIN ELECTROSURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 2009-06-12. The listed applicant is Kl Martin L.P.. The 510(k) number is K082505.

When did KLS MARTIN ELECTROSURGICAL INSTRUMENTS receive FDA 510(k) clearance?

KLS MARTIN ELECTROSURGICAL INSTRUMENTS received FDA 510(k) clearance on 2009-06-12, under 510(k) number K082505.

Who is the listed applicant for KLS MARTIN ELECTROSURGICAL INSTRUMENTS?

The FDA 510(k) record lists Kl Martin L.P. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KLS MARTIN ELECTROSURGICAL INSTRUMENTS?

The FDA product code for KLS MARTIN ELECTROSURGICAL INSTRUMENTS is GEI.

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Official Source

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