meddevicedb.com FDA Device Reference

TRIAGE B-TYPE NATRIURETIC PEPTIDE (BNP) CONTROLS

K000230 Class I Traditional
Decision Date
2000-02-29
Sponsor / Applicant
Biosite Incorporated

Technical Specification

510(k) Submission ID K000230
Product Code JJX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 2000-02-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRIAGE B-TYPE NATRIURETIC PEPTIDE (BNP) CONTROLS received FDA 510(k) clearance under submission number K000230, 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 2000-02-29.

Classification & Regulation

This clearance is catalogued under FDA product code JJX and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.