NO. 615 DETERMINATION OF CERULOPLASMIN IN SERUM— 510(k) K860138

Substantially Equivalent

Sigma Diagnostics, Inc.

FDA 510(k) clearance K860138 for NO. 615 DETERMINATION OF CERULOPLASMIN IN SERUM, Substantially Equivalent on 1986-03-28. Applicant: Sigma Diagnostics, Inc..

Clearance details

Applicant: Sigma Diagnostics, Inc.
Product code: Code DDB
Advisory panel: Immunology
Date received: 1986-01-14
Decision date: 1986-03-28
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.