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ELECTRO-CAUTERY SUCTION TUBE

K881413 Class II Traditional
Decision Date
1988-04-21
Sponsor / Applicant
Alto Development Corp.

Technical Specification

510(k) Submission ID K881413
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1988-04-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTRO-CAUTERY SUCTION TUBE received FDA 510(k) clearance under submission number K881413, sponsored by Alto Development 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 1988-04-21.

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.