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ORTHO*PAP-IA ENDOGENOUS ENZYME IMMUNO

K831670 Class II Traditional
Decision Date
1983-08-24
Sponsor / Applicant
Ortho Diagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K831670
Product Code JFH
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1020
Decision Date 1983-08-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORTHO*PAP-IA ENDOGENOUS ENZYME IMMUNO received FDA 510(k) clearance under submission number K831670, 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 1983-08-24.

Classification & Regulation

This clearance is catalogued under FDA product code JFH and 21 CFR 862.1020, within the Clinical Chemistry review panel as a Class II device.