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RFA/2 RAPID FLOW ANALYZER W/COMPUTER

K890332 Class I Traditional
Decision Date
1989-02-17
Sponsor / Applicant
Alpkem Corp.

Technical Specification

510(k) Submission ID K890332
Product Code JJC
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2150
Decision Date 1989-02-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RFA/2 RAPID FLOW ANALYZER W/COMPUTER received FDA 510(k) clearance under submission number K890332, sponsored by Alpkem Corp.. 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 1989-02-17.

Classification & Regulation

This clearance is catalogued under FDA product code JJC and 21 CFR 862.2150, within the Clinical Chemistry review panel as a Class I device.