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TANDEM-E TSH CALIBRATION VERIFICATION CONTROL SET

K912439 Class I Traditional
Decision Date
1991-08-28
Sponsor / Applicant
Hybritech, Inc.

Technical Specification

510(k) Submission ID K912439
Product Code JJX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1991-08-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TANDEM-E TSH CALIBRATION VERIFICATION CONTROL SET received FDA 510(k) clearance under submission number K912439, sponsored by Hybritech, 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 1991-08-28.

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.