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ACCESS TOTAL BHCG (5TH IS)

K130020 Class II Traditional
Decision Date
2013-10-01
Sponsor / Applicant
Beckman Coulter, Inc.

Technical Specification

510(k) Submission ID K130020
Product Code DHA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 2013-10-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACCESS TOTAL BHCG (5TH IS) received FDA 510(k) clearance under submission number K130020, 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 2013-10-01.

Classification & Regulation

This clearance is catalogued under FDA product code DHA and 21 CFR 862.1155, within the Clinical Chemistry review panel as a Class II device.