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TITAN GEL

K905149 Class II Traditional
Decision Date
1991-01-03
Sponsor / Applicant
Helena Laboratories

Technical Specification

510(k) Submission ID K905149
Product Code DAH
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 1991-01-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TITAN GEL received FDA 510(k) clearance under submission number K905149, sponsored by Helena Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1991-01-03.

Classification & Regulation

This clearance is catalogued under FDA product code DAH and 21 CFR 866.5510, within the Immunology review panel as a Class II device.