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FDA 510(k)

DAN MONOPOLAR LAP ACCESSORIES

K-Number: K052759 · 2006-06-14

Decision Date2006-06-14
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DAN MONOPOLAR LAP ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Dannoritzer Medizintechnik GmbH & Co. KG. It received FDA 510(k) clearance on 2006-06-14 under 510(k) number K052759. 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 DAN MONOPOLAR LAP ACCESSORIES?

DAN MONOPOLAR LAP ACCESSORIES is a medical device that received FDA 510(k) clearance on 2006-06-14. The listed applicant is Dannoritzer Medizintechnik GmbH & Co. KG. The 510(k) number is K052759.

When did DAN MONOPOLAR LAP ACCESSORIES receive FDA 510(k) clearance?

DAN MONOPOLAR LAP ACCESSORIES received FDA 510(k) clearance on 2006-06-14, under 510(k) number K052759.

Who is the listed applicant for DAN MONOPOLAR LAP ACCESSORIES?

The FDA 510(k) record lists Dannoritzer Medizintechnik GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DAN MONOPOLAR LAP ACCESSORIES?

The FDA product code for DAN MONOPOLAR LAP ACCESSORIES is GEI.

Related Clinical Trials

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.

Related Devices (Code: GEI)

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.

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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