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125I QUICK-MB TEST KIT FOR QUANTITATION

K821964 Class II Traditional
Decision Date
1982-07-22
Sponsor / Applicant
Intl. Immunoassay Laboratories, Inc.

Technical Specification

510(k) Submission ID K821964
Product Code JHT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1215
Decision Date 1982-07-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

125I QUICK-MB TEST KIT FOR QUANTITATION received FDA 510(k) clearance under submission number K821964, sponsored by Intl. Immunoassay Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1982-07-22.

Classification & Regulation

This clearance is catalogued under FDA product code JHT and 21 CFR 862.1215, within the Clinical Chemistry review panel as a Class II device.