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A&E MEDICAL ELECTROSURGICAL CONNECTING CORDS

K930528 Class II Traditional
Decision Date
1993-05-17
Sponsor / Applicant
Alto Development Corp.

Technical Specification

510(k) Submission ID K930528
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1993-05-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

A&E MEDICAL ELECTROSURGICAL CONNECTING CORDS received FDA 510(k) clearance under submission number K930528, 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 1993-05-17.

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.