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TBN-TIPPED OPTICAL FIBER

K952113 Class II Traditional
Decision Date
1995-06-01
Sponsor / Applicant
Myriad Lase, Inc.

Technical Specification

510(k) Submission ID K952113
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 1995-06-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TBN-TIPPED OPTICAL FIBER received FDA 510(k) clearance under submission number K952113, sponsored by Myriad Lase, 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 1995-06-01.

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.