meddevicedb.com FDA Device Reference

ACE T UPTAKE REAGENT TU CALIBRATORS

K981375 Class II Traditional
Decision Date
1998-06-10
Sponsor / Applicant
Schiapparelli Biosystems, Inc.

Technical Specification

510(k) Submission ID K981375
Product Code KHQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1715
Decision Date 1998-06-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACE T UPTAKE REAGENT TU CALIBRATORS received FDA 510(k) clearance under submission number K981375, sponsored by Schiapparelli Biosystems, 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 1998-06-10.

Classification & Regulation

This clearance is catalogued under FDA product code KHQ and 21 CFR 862.1715, within the Clinical Chemistry review panel as a Class II device.