meddevicedb.com FDA Device Reference

OPUS(R) PLUS ANALYZER

K913295 Class I Traditional
Decision Date
1991-09-11
Sponsor / Applicant
Pb Diagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K913295
Product Code JJQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2300
Decision Date 1991-09-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPUS(R) PLUS ANALYZER received FDA 510(k) clearance under submission number K913295, sponsored by Pb 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 1991-09-11.

Classification & Regulation

This clearance is catalogued under FDA product code JJQ and 21 CFR 862.2300, within the Clinical Chemistry review panel as a Class I device.