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MODEL E2517 AND MODEL E2503 POWER CONTROL PENCILS

K861112 Class II Traditional
Decision Date
1986-05-20
Sponsor / Applicant
Valleylab, Inc.

Technical Specification

510(k) Submission ID K861112
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1986-05-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL E2517 AND MODEL E2503 POWER CONTROL PENCILS received FDA 510(k) clearance under submission number K861112, sponsored by Valleylab, 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 1986-05-20.

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.