BIOPLEX 2200 EBV IGM PANEL ON BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEM— 510(k) K062213

Substantially Equivalent

Bio-Rad Laboratories, Inc.

FDA 510(k) clearance K062213 for BIOPLEX 2200 EBV IGM PANEL ON BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEM, Substantially Equivalent on 2006-12-08. Applicant: Bio-Rad Laboratories, Inc..

Clearance details

Applicant
Bio-Rad Laboratories, Inc.
Product code
Code LSE
Advisory panel
Microbiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Redmond, WA, US
Download summary PDFView on FDA.gov ↗

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