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 IDK842898
510k NumberK842898
Device Name:CURITY I.V. START KIT
ClassificationI.v. Start Kit
Applicant THE KENDAL CO. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeLRS  
CFR Regulation Number880.5200 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1984-07-23
Decision Date1984-08-17

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
20884527014665 K842898 000
20884527014658 K842898 000

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