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VENTREZYME PAP KIT IMMUNOASSAY PROSTATIC

K843230 Class II Traditional
Decision Date
1984-09-04
Sponsor / Applicant
Ventrex Laboratories, Inc.

Technical Specification

510(k) Submission ID K843230
Product Code JFH
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1020
Decision Date 1984-09-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VENTREZYME PAP KIT IMMUNOASSAY PROSTATIC received FDA 510(k) clearance under submission number K843230, sponsored by Ventrex 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 1984-09-04.

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.