510(k) K872750

LAKE CATHETER CARE KIT by Lake Medical Products, Inc. — Product Code KOD

K872750 is an FDA 510(k) premarket notification submitted by Lake Medical Products, Inc. for the device "LAKE CATHETER CARE KIT". The FDA issued a decision of Substantially Equivalent on September 3, 1987. The device falls under product code KOD (Catheter, Urological), a Class II device regulated under 21 CFR 876.5130. Lake Medical Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 3, 1987
Date Received
July 13, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Urological
Device Class
Class II
Regulation Number
876.5130
Review Panel
GU
Submission Type