meddevicedb.com FDA Device Reference

ADVANCED HAND HELD CO2 LASER MODEL HH-550 FOR SU

K864887 Class II Traditional
Decision Date
1987-04-10
Sponsor / Applicant
Bio Quantum Technologies, Inc.

Technical Specification

510(k) Submission ID K864887
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 1987-04-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVANCED HAND HELD CO2 LASER MODEL HH-550 FOR SU received FDA 510(k) clearance under submission number K864887, sponsored by Bio Quantum Technologies, 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 1987-04-10.

Classification & Regulation

This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.