Transfer Sets

Set, Transfer (blood/plasma)

Terumo Medical Corporation

The following data is part of a premarket notification filed by Terumo Medical Corporation with the FDA for Transfer Sets.

Pre-market Notification Details

Device IDBK860041
510k NumberBK860041
Device Name:Transfer Sets
ClassificationSet, Transfer (blood/plasma)
Applicant Terumo Medical Corporation 125 Blue Ball Road Elkton,  MD  21921
Product CodeKSB  
CFR Regulation Number864.9875 [🔎]
DecisionSubstantially Equivalent (SE)
Type510(k) Traditio
3rd Party ReviewedNo
Combination ProductNo
Date Received1987-03-10
Decision Date1987-06-01

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
05020583620032 BK860041 0
05020583620025 BK860041 0
05020583300026 BK860041 0

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