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TRIAGE STATMETER

K973547 Class I Traditional
Decision Date
1998-01-13
Sponsor / Applicant
Biosite Incorporated

Technical Specification

510(k) Submission ID K973547
Product Code KHO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2560
Decision Date 1998-01-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRIAGE STATMETER received FDA 510(k) clearance under submission number K973547, 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 1998-01-13.

Classification & Regulation

This clearance is catalogued under FDA product code KHO and 21 CFR 862.2560, within the Clinical Chemistry review panel as a Class I device.