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IMMPULSE T4 ASSAY REAGENTS

K875081 Class II Traditional
Decision Date
1988-02-11
Sponsor / Applicant
Sclavo, Inc.

Technical Specification

510(k) Submission ID K875081
Product Code CDX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1700
Decision Date 1988-02-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMMPULSE T4 ASSAY REAGENTS received FDA 510(k) clearance under submission number K875081, sponsored by Sclavo, 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 1988-02-11.

Classification & Regulation

This clearance is catalogued under FDA product code CDX and 21 CFR 862.1700, within the Clinical Chemistry review panel as a Class II device.