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FDA 510(k)

POWERGRIP BIPOLAR COAGULATION FORCEPS, MODEL 824XXXXX

K-Number: K033177 · 2004-03-11

ApplicantGunter Bissinger Medizintechnik GmbH
Decision Date2004-03-11
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

POWERGRIP BIPOLAR COAGULATION FORCEPS, MODEL 824XXXXX is the device name listed in this FDA 510(k) record. The listed applicant is Gunter Bissinger Medizintechnik GmbH. It received FDA 510(k) clearance on 2004-03-11 under 510(k) number K033177. 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 POWERGRIP BIPOLAR COAGULATION FORCEPS, MODEL 824XXXXX?

POWERGRIP BIPOLAR COAGULATION FORCEPS, MODEL 824XXXXX is a medical device that received FDA 510(k) clearance on 2004-03-11. The listed applicant is Gunter Bissinger Medizintechnik GmbH. The 510(k) number is K033177.

When did POWERGRIP BIPOLAR COAGULATION FORCEPS, MODEL 824XXXXX receive FDA 510(k) clearance?

POWERGRIP BIPOLAR COAGULATION FORCEPS, MODEL 824XXXXX received FDA 510(k) clearance on 2004-03-11, under 510(k) number K033177.

Who is the listed applicant for POWERGRIP BIPOLAR COAGULATION FORCEPS, MODEL 824XXXXX?

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

What is the FDA product code for POWERGRIP BIPOLAR COAGULATION FORCEPS, MODEL 824XXXXX?

The FDA product code for POWERGRIP BIPOLAR COAGULATION FORCEPS, MODEL 824XXXXX is HET.

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.

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Other records listing Gunter Bissinger Medizintechnik 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.

K172368Bipolar Micro-Coagulation Forceps

Related Devices (Code: HET)

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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