Transfer Sets

Set, Transfer (blood/plasma)

Cytosol Laboratories, Inc.

The following data is part of a premarket notification filed by Cytosol Laboratories, Inc. with the FDA for Transfer Sets.

Pre-market Notification Details

• Device ID: BK950060
• 510k Number: BK950060
• Device Name: Transfer Sets
• Classification: Set, Transfer (blood/plasma)
• Applicant: Cytosol Laboratories, Inc. 55 Messina Drive Braintree, MA 02184 US
• 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: 1995-10-27
• Decision Date: 1996-11-25

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00887868260285	BK950060	0