meddevicedb.com FDA Device Reference

FLOW-PAC INORGANIC PHOSPHORUS REAGENTS

K871321 Class I Traditional
Decision Date
1987-04-22
Sponsor / Applicant
American Research Products Co.

Technical Specification

510(k) Submission ID K871321
Product Code CEO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1580
Decision Date 1987-04-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLOW-PAC INORGANIC PHOSPHORUS REAGENTS received FDA 510(k) clearance under submission number K871321, sponsored by American Research Products Co.. 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 1987-04-22.

Classification & Regulation

This clearance is catalogued under FDA product code CEO and 21 CFR 862.1580, within the Clinical Chemistry review panel as a Class I device.