510(k) K925281

KIT PAK URINARY CARE SUPPLIES by Kit Pak, Inc. — Product Code KNY

K925281 is an FDA 510(k) premarket notification submitted by Kit Pak, Inc. for the device "KIT PAK URINARY CARE SUPPLIES". The FDA issued a decision of Substantially Equivalent (kit) on April 19, 1993. The device falls under product code KNY (Accessories, Catheter, G-U), a Class II device regulated under 21 CFR 876.5130. Kit Pak, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESK (Substantially Equivalent (kit))
Decision Date
April 19, 1993
Date Received
October 20, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Accessories, Catheter, G-U
Device Class
Class II
Regulation Number
876.5130
Review Panel
GU
Submission Type