meddevicedb.com FDA Device Reference

QUALITATIVE ENZYME IMMUNOASSAY-DETECT

K832905 Class II Traditional
Decision Date
1984-02-03
Sponsor / Applicant
Btc Diagnostics, Inc.

Technical Specification

510(k) Submission ID K832905
Product Code LCX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 1984-02-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUALITATIVE ENZYME IMMUNOASSAY-DETECT received FDA 510(k) clearance under submission number K832905, sponsored by Btc Diagnostics, 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 1984-02-03.

Classification & Regulation

This clearance is catalogued under FDA product code LCX and 21 CFR 862.1155, within the Clinical Chemistry review panel as a Class II device.