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 ID: BK860041
• 510k Number: BK860041
• Device Name: Transfer Sets
• Classification: Set, Transfer (blood/plasma)
• Applicant: Terumo Medical Corporation 125 Blue Ball Road Elkton, MD 21921
• Product Code: KSB
• CFR Regulation Number: 864.9875 [🔎]
• Decision: Substantially Equivalent (SE)
• Type: 510(k) Traditio
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1987-03-10
• Decision Date: 1987-06-01

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
05020583620032	BK860041	0
05020583620025	BK860041	0
05020583300026	BK860041	0