510(k) K855076

ANGIOMED URETER DIATION SETS by Angiomed U.S., Inc. — Product Code KOD

K855076 is an FDA 510(k) premarket notification submitted by Angiomed U.S., Inc. for the device "ANGIOMED URETER DIATION SETS". The FDA issued a decision of Substantially Equivalent on March 11, 1986. The device falls under product code KOD (Catheter, Urological), a Class II device regulated under 21 CFR 876.5130. Angiomed U.S., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 11, 1986
Date Received
December 19, 1985
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