meddevicedb.com FDA Device Reference

PRECEPT MICRO-GARD LASER MASK

K891409 Class II Traditional
Decision Date
1989-04-07
Sponsor / Applicant
Mars White Knight

Technical Specification

510(k) Submission ID K891409
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1989-04-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PRECEPT MICRO-GARD LASER MASK received FDA 510(k) clearance under submission number K891409, sponsored by Mars White Knight. 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 1989-04-07.

Classification & Regulation

This clearance is catalogued under FDA product code FXX and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class II device.