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ARCHITECT T-UPTAKE CALIBRATORS (A-F) AND CONTROLS (LOW, HIGH)

K042307 Class II Abbreviated
Decision Date
2004-11-03
Sponsor / Applicant
Seradyn, Inc.

Technical Specification

510(k) Submission ID K042307
Product Code JIT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1150
Decision Date 2004-11-03
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ARCHITECT T-UPTAKE CALIBRATORS (A-F) AND CONTROLS (LOW, HIGH) received FDA 510(k) clearance under submission number K042307, sponsored by Seradyn, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2004-11-03.

Classification & Regulation

This clearance is catalogued under FDA product code JIT and 21 CFR 862.1150, within the Clinical Chemistry review panel as a Class II device.