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NOVOCHECK/CHECKPOINT/CONTROL SOLUTION

K872049 Class II Traditional
Decision Date
1987-08-13
Sponsor / Applicant
Garid, Inc.

Technical Specification

510(k) Submission ID K872049
Product Code CGA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 1987-08-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NOVOCHECK/CHECKPOINT/CONTROL SOLUTION received FDA 510(k) clearance under submission number K872049, sponsored by Garid, Inc.. 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 1987-08-13.

Classification & Regulation

This clearance is catalogued under FDA product code CGA and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.