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FDA 510(k)

BITECH BIPOLAR SCISSORS

K-Number: K042077 · 2004-10-27

ApplicantGuenter Bissinger Medizintechnik GmbH
Decision Date2004-10-27
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BITECH BIPOLAR SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Guenter Bissinger Medizintechnik GmbH. It received FDA 510(k) clearance on 2004-10-27 under 510(k) number K042077. 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 BITECH BIPOLAR SCISSORS?

BITECH BIPOLAR SCISSORS is a medical device that received FDA 510(k) clearance on 2004-10-27. The listed applicant is Guenter Bissinger Medizintechnik GmbH. The 510(k) number is K042077.

When did BITECH BIPOLAR SCISSORS receive FDA 510(k) clearance?

BITECH BIPOLAR SCISSORS received FDA 510(k) clearance on 2004-10-27, under 510(k) number K042077.

Who is the listed applicant for BITECH BIPOLAR SCISSORS?

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

What is the FDA product code for BITECH BIPOLAR SCISSORS?

The FDA product code for BITECH BIPOLAR SCISSORS is GEI.

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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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