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HCG SCREENING TEST

K830156 Class II Traditional
Decision Date
1983-02-09
Sponsor / Applicant
Tago, Inc.

Technical Specification

510(k) Submission ID K830156
Product Code JHJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 1983-02-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HCG SCREENING TEST received FDA 510(k) clearance under submission number K830156, sponsored by Tago, 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 1983-02-09.

Classification & Regulation

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