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BIOSCANNER CREATININE TEST STRIPS

K010456 Class II Traditional
Decision Date
2001-06-20
Sponsor / Applicant
Polymer Technology Systems, Inc.

Technical Specification

510(k) Submission ID K010456
Product Code JFY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1225
Decision Date 2001-06-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOSCANNER CREATININE TEST STRIPS received FDA 510(k) clearance under submission number K010456, sponsored by Polymer Technology Systems, 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 2001-06-20.

Classification & Regulation

This clearance is catalogued under FDA product code JFY and 21 CFR 862.1225, within the Clinical Chemistry review panel as a Class II device.