CURITY I.V. START KIT

I.v. Start Kit

THE KENDAL CO.

The following data is part of a premarket notification filed by The Kendal Co. with the FDA for Curity I.v. Start Kit.

Pre-market Notification Details

• Device ID: K842898
• 510k Number: K842898
• Device Name: CURITY I.V. START KIT
• Classification: I.v. Start Kit
• Applicant: THE KENDAL CO. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: LRS
• CFR Regulation Number: 880.5200 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1984-07-23
• Decision Date: 1984-08-17

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
20884527014665	K842898	000
20884527014658	K842898	000