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ACE -GT REAGENT; ACE LIPASE RAGENT; ACE T4 REAGENT

K131515 Class II Traditional
Decision Date
2013-08-14
Sponsor / Applicant
Alfa Wassermann

Technical Specification

510(k) Submission ID K131515
Product Code KLI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1700
Decision Date 2013-08-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACE -GT REAGENT; ACE LIPASE RAGENT; ACE T4 REAGENT received FDA 510(k) clearance under submission number K131515, sponsored by Alfa Wassermann. 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 2013-08-14.

Classification & Regulation

This clearance is catalogued under FDA product code KLI and 21 CFR 862.1700, within the Clinical Chemistry review panel as a Class II device.