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FDA 510(k)

ELECTROSURGICAL LOOP ELECTRODE

K-Number: K940191 · 1994-12-30

Decision Date1994-12-30
Product CodeHGI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL LOOP ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is National Wire & Stamping, Inc.. It received FDA 510(k) clearance on 1994-12-30 under 510(k) number K940191. The device is classified under product code HGI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROSURGICAL LOOP ELECTRODE?

ELECTROSURGICAL LOOP ELECTRODE is a medical device that received FDA 510(k) clearance on 1994-12-30. The listed applicant is National Wire & Stamping, Inc.. The 510(k) number is K940191.

When did ELECTROSURGICAL LOOP ELECTRODE receive FDA 510(k) clearance?

ELECTROSURGICAL LOOP ELECTRODE received FDA 510(k) clearance on 1994-12-30, under 510(k) number K940191.

Who is the listed applicant for ELECTROSURGICAL LOOP ELECTRODE?

The FDA 510(k) record lists National Wire & Stamping, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTROSURGICAL LOOP ELECTRODE?

The FDA product code for ELECTROSURGICAL LOOP ELECTRODE is HGI.

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 National Wire & Stamping, 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.

Related Devices (Code: HGI)

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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