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IQ CALCIUM

K891217 Class II Traditional
Decision Date
1989-05-03
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K891217
Product Code CIC
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1145
Decision Date 1989-05-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IQ CALCIUM received FDA 510(k) clearance under submission number K891217, sponsored by Bd Becton Dickinson Vacutainer Systems Preanalytic. 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 1989-05-03.

Classification & Regulation

This clearance is catalogued under FDA product code CIC and 21 CFR 862.1145, within the Clinical Chemistry review panel as a Class II device.