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DRI-STAT ACID PHOSPHATASE REAGENT

K053612 Class II Traditional
Decision Date
2006-04-26
Sponsor / Applicant
Beckman Coulter, Inc.

Technical Specification

510(k) Submission ID K053612
Product Code CKB
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1020
Decision Date 2006-04-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DRI-STAT ACID PHOSPHATASE REAGENT received FDA 510(k) clearance under submission number K053612, sponsored by Beckman Coulter, 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 2006-04-26.

Classification & Regulation

This clearance is catalogued under FDA product code CKB and 21 CFR 862.1020, within the Clinical Chemistry review panel as a Class II device.