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MDT UNISPORE AND SPOR-TEST BIOLOGICALINDICATOR

K960777 Class II Traditional
Decision Date
1996-05-23
Sponsor / Applicant
Mdt Corp., Inc.

Technical Specification

510(k) Submission ID K960777
Product Code FRC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 1996-05-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MDT UNISPORE AND SPOR-TEST BIOLOGICALINDICATOR received FDA 510(k) clearance under submission number K960777, sponsored by Mdt Corp., Inc.. 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 1996-05-23.

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.