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MTM BIOSCANNER K TEST STRIPS

K981865 Class I Traditional
Decision Date
1999-02-26
Sponsor / Applicant
Polymer Technology Systems, Inc.

Technical Specification

510(k) Submission ID K981865
Product Code JMK
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1380
Decision Date 1999-02-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MTM BIOSCANNER K TEST STRIPS received FDA 510(k) clearance under submission number K981865, 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 1999-02-26.

Classification & Regulation

This clearance is catalogued under FDA product code JMK and 21 CFR 862.1380, within the Clinical Chemistry review panel as a Class I device.