SIGMA PROCEDURE NO. 333-UV— 510(k) K914777

Substantially Equivalent

Sigma Diagnostics, Inc.

FDA 510(k) clearance K914777 for SIGMA PROCEDURE NO. 333-UV, Substantially Equivalent on 1991-12-27. Applicant: Sigma Diagnostics, Inc..

Clearance details

Applicant: Sigma Diagnostics, Inc.
Product code: Code DML
Advisory panel: Clinical Toxicology
Date received: 1991-10-23
Decision date: 1991-12-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.