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FDA 510(k)

PMC LAPAROSCOPIC INSTRUMENTS

K-Number: K101193 · 2010-10-18

ApplicantPmc Medical GmbH
Decision Date2010-10-18
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PMC LAPAROSCOPIC INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Pmc Medical GmbH. It received FDA 510(k) clearance on 2010-10-18 under 510(k) number K101193. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PMC LAPAROSCOPIC INSTRUMENTS?

PMC LAPAROSCOPIC INSTRUMENTS is a medical device that received FDA 510(k) clearance on 2010-10-18. The listed applicant is Pmc Medical GmbH. The 510(k) number is K101193.

When did PMC LAPAROSCOPIC INSTRUMENTS receive FDA 510(k) clearance?

PMC LAPAROSCOPIC INSTRUMENTS received FDA 510(k) clearance on 2010-10-18, under 510(k) number K101193.

Who is the listed applicant for PMC LAPAROSCOPIC INSTRUMENTS?

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

What is the FDA product code for PMC LAPAROSCOPIC INSTRUMENTS?

The FDA product code for PMC LAPAROSCOPIC INSTRUMENTS is GCJ.

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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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