meddevicedb.com FDA Device Reference

UBI MAGIWEL PAP (PROSTATIC ACID PHOSPHATASE) EIA QUANTITATVE

K981573 Class II Traditional
Decision Date
1998-09-15
Sponsor / Applicant
United Biotech, Inc.

Technical Specification

510(k) Submission ID K981573
Product Code JFH
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1020
Decision Date 1998-09-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UBI MAGIWEL PAP (PROSTATIC ACID PHOSPHATASE) EIA QUANTITATVE received FDA 510(k) clearance under submission number K981573, sponsored by United Biotech, 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 1998-09-15.

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.