meddevicedb.com FDA Device Reference

TINA-QUANT MICROALBUMIN

K932950 Class I Traditional
Decision Date
1995-02-10
Sponsor / Applicant
Boehringer Mannheim Corp.

Technical Specification

510(k) Submission ID K932950
Product Code JIR
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1645
Decision Date 1995-02-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TINA-QUANT MICROALBUMIN received FDA 510(k) clearance under submission number K932950, sponsored by Boehringer Mannheim Corp.. 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 1995-02-10.

Classification & Regulation

This clearance is catalogued under FDA product code JIR and 21 CFR 862.1645, within the Clinical Chemistry review panel as a Class I device.