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FDA 510(k)

SURGICAL ELECTRICAL PENCIL

K-Number: K913623 · 1992-02-21

ApplicantAaron Medical, Inc.
Decision Date1992-02-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL ELECTRICAL PENCIL is the device name listed in this FDA 510(k) record. The listed applicant is Aaron Medical, Inc.. It received FDA 510(k) clearance on 1992-02-21 under 510(k) number K913623. 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 SURGICAL ELECTRICAL PENCIL?

SURGICAL ELECTRICAL PENCIL is a medical device that received FDA 510(k) clearance on 1992-02-21. The listed applicant is Aaron Medical, Inc.. The 510(k) number is K913623.

When did SURGICAL ELECTRICAL PENCIL receive FDA 510(k) clearance?

SURGICAL ELECTRICAL PENCIL received FDA 510(k) clearance on 1992-02-21, under 510(k) number K913623.

Who is the listed applicant for SURGICAL ELECTRICAL PENCIL?

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

What is the FDA product code for SURGICAL ELECTRICAL PENCIL?

The FDA product code for SURGICAL ELECTRICAL PENCIL is GEI.

Related Clinical Trials

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Other records listing Aaron Medical, 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.

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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.

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Official Source

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