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TRAVASPORE BIOLOGICAL INDICATOR

K832922 Class II Traditional
Decision Date
1983-11-21
Sponsor / Applicant
Travenol Laboratories, S.A.

Technical Specification

510(k) Submission ID K832922
Product Code FRC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 1983-11-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRAVASPORE BIOLOGICAL INDICATOR received FDA 510(k) clearance under submission number K832922, sponsored by Travenol Laboratories, S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1983-11-21.

Classification & Regulation

This clearance is catalogued under FDA product code FRC and 21 CFR 880.2800, within the General Hospital review panel as a Class II device.