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COMBI SCAN 500 URINE TEST STRIP ANALYZER, MODEL A93005

K061812 Class II Traditional
Decision Date
2007-04-06
Sponsor / Applicant
Analyticon Biotechnologies AG

Technical Specification

510(k) Submission ID K061812
Product Code JIL
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1340
Decision Date 2007-04-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMBI SCAN 500 URINE TEST STRIP ANALYZER, MODEL A93005 received FDA 510(k) clearance under submission number K061812, sponsored by Analyticon Biotechnologies AG. 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 2007-04-06.

Classification & Regulation

This clearance is catalogued under FDA product code JIL and 21 CFR 862.1340, within the Clinical Chemistry review panel as a Class II device.