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FDA 510(k)

PRECISION BIPOLAR COAGULATOR

K-Number: K951985 · 1995-05-23

Decision Date1995-05-23
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PRECISION BIPOLAR COAGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Valley Forge Scientific Corp.. It received FDA 510(k) clearance on 1995-05-23 under 510(k) number K951985. 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 PRECISION BIPOLAR COAGULATOR?

PRECISION BIPOLAR COAGULATOR is a medical device that received FDA 510(k) clearance on 1995-05-23. The listed applicant is Valley Forge Scientific Corp.. The 510(k) number is K951985.

When did PRECISION BIPOLAR COAGULATOR receive FDA 510(k) clearance?

PRECISION BIPOLAR COAGULATOR received FDA 510(k) clearance on 1995-05-23, under 510(k) number K951985.

Who is the listed applicant for PRECISION BIPOLAR COAGULATOR?

The FDA 510(k) record lists Valley Forge Scientific Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRECISION BIPOLAR COAGULATOR?

The FDA product code for PRECISION BIPOLAR COAGULATOR 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 Valley Forge Scientific Corp. 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 27 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

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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