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COMPLEMENT CONTROL

K960874 Class I Traditional
Decision Date
1996-06-14
Sponsor / Applicant
Wako Chemicals USA, Inc.

Technical Specification

510(k) Submission ID K960874
Product Code JJX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1996-06-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMPLEMENT CONTROL received FDA 510(k) clearance under submission number K960874, sponsored by Wako Chemicals USA, 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 1996-06-14.

Classification & Regulation

This clearance is catalogued under FDA product code JJX and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.