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T3 STI KIT

K780146 Class II Traditional
Decision Date
1978-02-23
Sponsor / Applicant
Polysciences, Inc.

Technical Specification

510(k) Submission ID K780146
Product Code KHQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1715
Decision Date 1978-02-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

T3 STI KIT received FDA 510(k) clearance under submission number K780146, sponsored by Polysciences, 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 1978-02-23.

Classification & Regulation

This clearance is catalogued under FDA product code KHQ and 21 CFR 862.1715, within the Clinical Chemistry review panel as a Class II device.