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SURGICAL ELECTRICAL PENCIL

K913623 Class II Traditional
Decision Date
1992-02-21
Sponsor / Applicant
Aaron Medical, Inc.

Technical Specification

510(k) Submission ID K913623
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1992-02-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL ELECTRICAL PENCIL received FDA 510(k) clearance under submission number K913623, sponsored by Aaron Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1992-02-21.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.