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SERIES SY DISPOSABLE ELECTROSURGICAL PAD

K082204 Class II Traditional
Decision Date
2008-08-13
Sponsor / Applicant
Ventlab Corp.

Technical Specification

510(k) Submission ID K082204
Product Code ODR
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2008-08-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SERIES SY DISPOSABLE ELECTROSURGICAL PAD received FDA 510(k) clearance under submission number K082204, sponsored by Ventlab Corp.. 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 2008-08-13.

Classification & Regulation

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