meddevicedb.com FDA Device Reference

CAUTERY; LOW TEMPERATURE (FINEADJUSTABLE FINE TIP, ELONGATED FINE TIP, MICRO FINE TIP)

K121441 Class II Traditional
Decision Date
2012-07-20
Sponsor / Applicant
Bovie Medical Corporation

Technical Specification

510(k) Submission ID K121441
Product Code HQP
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.4115
Decision Date 2012-07-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CAUTERY; LOW TEMPERATURE (FINEADJUSTABLE FINE TIP, ELONGATED FINE TIP, MICRO FINE TIP) received FDA 510(k) clearance under submission number K121441, sponsored by Bovie Medical Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2012-07-20.

Classification & Regulation

This clearance is catalogued under FDA product code HQP and 21 CFR 886.4115, within the Ophthalmic review panel as a Class II device.