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TRIAGE BNP TEST FOR THE BECKMAN COULTER IMMUNOASSAY SYSTEMS, MODEL CATALOG #98200

K033383 Class II Traditional
Decision Date
2003-12-23
Sponsor / Applicant
Biosite Incorporated

Technical Specification

510(k) Submission ID K033383
Product Code NBC
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1117
Decision Date 2003-12-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRIAGE BNP TEST FOR THE BECKMAN COULTER IMMUNOASSAY SYSTEMS, MODEL CATALOG #98200 received FDA 510(k) clearance under submission number K033383, sponsored by Biosite Incorporated. 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 2003-12-23.

Classification & Regulation

This clearance is catalogued under FDA product code NBC and 21 CFR 862.1117, within the Clinical Chemistry review panel as a Class II device.