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ORTHO B-HCG SLIDE TEST FOR PREGNANCY

K833137 Class II Traditional
Decision Date
1984-01-18
Sponsor / Applicant
Ortho Diagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K833137
Product Code JHJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 1984-01-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORTHO B-HCG SLIDE TEST FOR PREGNANCY received FDA 510(k) clearance under submission number K833137, sponsored by Ortho Diagnostic Systems, 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 1984-01-18.

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.