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FDA 510(k)

ELECTROSURGICAL BIPOLAR FORCEPS

K-Number: K903006 · 1990-09-20

Decision Date1990-09-20
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL BIPOLAR FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Megadyne Medical Products, Inc.. It received FDA 510(k) clearance on 1990-09-20 under 510(k) number K903006. 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 ELECTROSURGICAL BIPOLAR FORCEPS?

ELECTROSURGICAL BIPOLAR FORCEPS is a medical device that received FDA 510(k) clearance on 1990-09-20. The listed applicant is Megadyne Medical Products, Inc.. The 510(k) number is K903006.

When did ELECTROSURGICAL BIPOLAR FORCEPS receive FDA 510(k) clearance?

ELECTROSURGICAL BIPOLAR FORCEPS received FDA 510(k) clearance on 1990-09-20, under 510(k) number K903006.

Who is the listed applicant for ELECTROSURGICAL BIPOLAR FORCEPS?

The FDA 510(k) record lists Megadyne Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTROSURGICAL BIPOLAR FORCEPS?

The FDA product code for ELECTROSURGICAL BIPOLAR FORCEPS 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.

Other records listing Megadyne Medical Products, Inc. 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.

View all 48 devices →

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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