TINA-QUANT CERULOPLASMIN— 510(k) K091741

Substantially Equivalent

Roche Diagnostics

FDA 510(k) clearance K091741 for TINA-QUANT CERULOPLASMIN, Substantially Equivalent on 2010-03-18. Applicant: Roche Diagnostics. Device class: 2.

Clearance details

Applicant
Roche Diagnostics
Product code
Code CHN
Device class
Class 2
Regulation
21 CFR 866.5210
Advisory panel
Immunology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Indianapolis, IN, US
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