Automated Blood Cell Separators

Separator, Automated, Blood Cell, Diagnostic

Cobe Laboratories, Inc.

The following data is part of a premarket notification filed by Cobe Laboratories, Inc. with the FDA for Automated Blood Cell Separators.

Pre-market Notification Details

Device IDBK950030
510k NumberBK950030
Device Name:Automated Blood Cell Separators
ClassificationSeparator, Automated, Blood Cell, Diagnostic
Applicant Cobe Laboratories, Inc. 1185 Oak Street Lakewood,  CO  80215
Product CodeGKT  
CFR Regulation Number864.9245 [🔎]
DecisionSubstantially Equivalent (SE)
Type510(k) Traditio
3rd Party ReviewedNo
Combination ProductNo
Date Received1995-05-05
Decision Date1996-02-15

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