meddevicedb.com FDA Device Reference

MODEL 8750 BIPOLAR/MONOPOLAR ELECTROSURGICAL GENE.

K895841 Class II Traditional
Decision Date
1989-11-15
Sponsor / Applicant
Everest Medical Corp.

Technical Specification

510(k) Submission ID K895841
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 1989-11-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 8750 BIPOLAR/MONOPOLAR ELECTROSURGICAL GENE. received FDA 510(k) clearance under submission number K895841, sponsored by Everest Medical 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 1989-11-15.

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.