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FDA 510(k)

MINI-SYMM BIPOLAR COAGULATOR

K-Number: K964143 · 1997-01-09

ApplicantValley Forge Scientific Corp.
Decision Date1997-01-09
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MINI-SYMM 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 1997-01-09 under 510(k) number K964143. 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 MINI-SYMM BIPOLAR COAGULATOR?

MINI-SYMM BIPOLAR COAGULATOR is a medical device that received FDA 510(k) clearance on 1997-01-09. The listed applicant is Valley Forge Scientific Corp.. The 510(k) number is K964143.

When did MINI-SYMM BIPOLAR COAGULATOR receive FDA 510(k) clearance?

MINI-SYMM BIPOLAR COAGULATOR received FDA 510(k) clearance on 1997-01-09, under 510(k) number K964143.

Who is the listed applicant for MINI-SYMM 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 MINI-SYMM BIPOLAR COAGULATOR?

The FDA product code for MINI-SYMM BIPOLAR COAGULATOR is GEI.

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Other records listing Valley Forge Scientific Corp. as applicant

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K050364MALIS 2000 BIPOLAR ELECTROSURGICAL SYSTEMK042604VALLY FORGE SCIENTIFIC MALIS BIPOLAR DISPOSABLE FINGER OPERATED ELECTROSURGICAL INSTRUMENTSK032601STRYKER INTERVENTIONAL PAIN RF GENERATORK033499MALIS IRRIGATION MODULE 1000K982229BI-DENTK973554VALLEY FORGE BIPOLAR BALL TIP ELECTRODE

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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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