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FDA 510(k)

ELECTROSURGICAL CAULTERY PENCIL

K-Number: K830532 · 1983-04-27

Decision Date1983-04-27
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL CAULTERY PENCIL is the device name listed in this FDA 510(k) record. The listed applicant is American V. Mueller. It received FDA 510(k) clearance on 1983-04-27 under 510(k) number K830532. 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 CAULTERY PENCIL?

ELECTROSURGICAL CAULTERY PENCIL is a medical device that received FDA 510(k) clearance on 1983-04-27. The listed applicant is American V. Mueller. The 510(k) number is K830532.

When did ELECTROSURGICAL CAULTERY PENCIL receive FDA 510(k) clearance?

ELECTROSURGICAL CAULTERY PENCIL received FDA 510(k) clearance on 1983-04-27, under 510(k) number K830532.

Who is the listed applicant for ELECTROSURGICAL CAULTERY PENCIL?

The FDA 510(k) record lists American V. Mueller as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTROSURGICAL CAULTERY PENCIL?

The FDA product code for ELECTROSURGICAL CAULTERY PENCIL 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 American V. Mueller 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 31 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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