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FDA 510(k)

LAPAROSCOPIC AND ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES, LAPAROSCOPY RUDOLF SYSTEM

K-Number: K073498 · 2008-09-19

ApplicantRudolf Medical GmbH + Co. KG
Decision Date2008-09-19
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC AND ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES, LAPAROSCOPY RUDOLF SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Rudolf Medical GmbH + Co. KG. It received FDA 510(k) clearance on 2008-09-19 under 510(k) number K073498. 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 LAPAROSCOPIC AND ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES, LAPAROSCOPY RUDOLF SYSTEM?

LAPAROSCOPIC AND ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES, LAPAROSCOPY RUDOLF SYSTEM is a medical device that received FDA 510(k) clearance on 2008-09-19. The listed applicant is Rudolf Medical GmbH + Co. KG. The 510(k) number is K073498.

When did LAPAROSCOPIC AND ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES, LAPAROSCOPY RUDOLF SYSTEM receive FDA 510(k) clearance?

LAPAROSCOPIC AND ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES, LAPAROSCOPY RUDOLF SYSTEM received FDA 510(k) clearance on 2008-09-19, under 510(k) number K073498.

Who is the listed applicant for LAPAROSCOPIC AND ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES, LAPAROSCOPY RUDOLF SYSTEM?

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

What is the FDA product code for LAPAROSCOPIC AND ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES, LAPAROSCOPY RUDOLF SYSTEM?

The FDA product code for LAPAROSCOPIC AND ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES, LAPAROSCOPY RUDOLF SYSTEM is GEI.

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Official Source

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