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FDA 510(k)

COAGULATOR, LAPAROSCOPIC, LUNIPOLAR/ACCESSORIES

K-Number: K933768 · 1994-06-27

ApplicantMahe-Medizintechnik
Decision Date1994-06-27
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

COAGULATOR, LAPAROSCOPIC, LUNIPOLAR/ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Mahe-Medizintechnik. It received FDA 510(k) clearance on 1994-06-27 under 510(k) number K933768. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COAGULATOR, LAPAROSCOPIC, LUNIPOLAR/ACCESSORIES?

COAGULATOR, LAPAROSCOPIC, LUNIPOLAR/ACCESSORIES is a medical device that received FDA 510(k) clearance on 1994-06-27. The listed applicant is Mahe-Medizintechnik. The 510(k) number is K933768.

When did COAGULATOR, LAPAROSCOPIC, LUNIPOLAR/ACCESSORIES receive FDA 510(k) clearance?

COAGULATOR, LAPAROSCOPIC, LUNIPOLAR/ACCESSORIES received FDA 510(k) clearance on 1994-06-27, under 510(k) number K933768.

Who is the listed applicant for COAGULATOR, LAPAROSCOPIC, LUNIPOLAR/ACCESSORIES?

The FDA 510(k) record lists Mahe-Medizintechnik as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COAGULATOR, LAPAROSCOPIC, LUNIPOLAR/ACCESSORIES?

The FDA product code for COAGULATOR, LAPAROSCOPIC, LUNIPOLAR/ACCESSORIES is HET.

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Other records listing Mahe-Medizintechnik 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.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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