SIGMA DIAGNOSTICS BUN REAGENT— 510(k) K963537

Substantially Equivalent

Sigma Diagnostics, Inc.

FDA 510(k) clearance K963537 for SIGMA DIAGNOSTICS BUN REAGENT, Substantially Equivalent on 1996-10-24. Applicant: Sigma Diagnostics, Inc..

Clearance details

Applicant: Sigma Diagnostics, Inc.
Product code: Code LFP
Advisory panel: Clinical Chemistry
Date received: 1996-09-04
Decision date: 1996-10-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, US

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