Cleared Traditional

K983860 - MTM BIOSCANNER K TEST STRIPS, CAT # BSA610 (FDA 510(k) Clearance)

Dec 1999
Decision
420d
Days
Class 1
Risk

K983860 is an FDA 510(k) clearance for the MTM BIOSCANNER K TEST STRIPS, CAT # BSA610. This device is classified as a Acid, Alpha-ketobutyric And Nadh (u.v.), Hydroxybutyric Dehydrogenase (Class I - General Controls, product code JMK).

Submitted by Polymer Technology Systems, Inc. (Indianapolis, US). The FDA issued a Cleared decision on December 27, 1999, 420 days after receiving the submission on November 2, 1998.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1380.

Submission Details

510(k) Number K983860 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 02, 1998
Decision Date December 27, 1999
Days to Decision 420 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Statement

Device Classification

Product Code JMK — Acid, Alpha-ketobutyric And Nadh (u.v.), Hydroxybutyric Dehydrogenase
Device Class Class I - General Controls
CFR Regulation 21 CFR 862.1380

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