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FDA 510(k)

HANS HERMANN LAPAROSCOPES AND ACCESSORIES

K-Number: K051610 · 2005-07-29

ApplicantHans Hermann GmbH
Decision Date2005-07-29
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HANS HERMANN LAPAROSCOPES AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Hans Hermann GmbH. It received FDA 510(k) clearance on 2005-07-29 under 510(k) number K051610. 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 HANS HERMANN LAPAROSCOPES AND ACCESSORIES?

HANS HERMANN LAPAROSCOPES AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2005-07-29. The listed applicant is Hans Hermann GmbH. The 510(k) number is K051610.

When did HANS HERMANN LAPAROSCOPES AND ACCESSORIES receive FDA 510(k) clearance?

HANS HERMANN LAPAROSCOPES AND ACCESSORIES received FDA 510(k) clearance on 2005-07-29, under 510(k) number K051610.

Who is the listed applicant for HANS HERMANN LAPAROSCOPES AND ACCESSORIES?

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

What is the FDA product code for HANS HERMANN LAPAROSCOPES AND ACCESSORIES?

The FDA product code for HANS HERMANN LAPAROSCOPES AND ACCESSORIES is GCJ.

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Other records listing Hans Hermann 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.

K983535THE TITANIUM MINIPLATING SYSTEM, THE TITANIUM MICROPLATING SYSTEM, THE TITANIUM MEDIUMPLATING SYSTEM, MODEL #'S H12-1010

Related Devices (Code: GCJ)

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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