meddevicedb.com FDA Device Reference

ELITE #MPS 101 ELECTROSURGICAL SWITCH

K822070 Class II Traditional
Decision Date
1982-08-19
Sponsor / Applicant
Delta Medical Electronics, Inc.

Technical Specification

510(k) Submission ID K822070
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1982-08-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELITE #MPS 101 ELECTROSURGICAL SWITCH received FDA 510(k) clearance under submission number K822070, sponsored by Delta Medical Electronics, 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 1982-08-19.

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.