BIOPOOL PROTEIN C EID KIT AND BULK PLATES

Test, Qualitative And Quantitative Factor Deficiency

BIOPOOL AB

The following data is part of a premarket notification filed by Biopool Ab with the FDA for Biopool Protein C Eid Kit And Bulk Plates.

Pre-market Notification Details

Device IDK902566
510k NumberK902566
Device Name:BIOPOOL PROTEIN C EID KIT AND BULK PLATES
ClassificationTest, Qualitative And Quantitative Factor Deficiency
Applicant BIOPOOL AB 1016 SUTTON DR. UNIT C8, BURLINGTON Ontario, L7l 6b8,  CA L7l 6b8
ContactCerskus, Phd
CorrespondentCerskus, Phd
BIOPOOL AB 1016 SUTTON DR. UNIT C8, BURLINGTON Ontario, L7l 6b8,  CA L7l 6b8
Product CodeGGP  
CFR Regulation Number864.7290 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1990-06-11
Decision Date1990-08-09

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