510(k) K874517

PHARMASEAL RUBBER URETHRAL CATHETER by American Pharmaseal Div. Ahsc — Product Code KOD

K874517 is an FDA 510(k) premarket notification submitted by American Pharmaseal Div. Ahsc for the device "PHARMASEAL RUBBER URETHRAL CATHETER". The FDA issued a decision of Substantially Equivalent on December 3, 1987. The device falls under product code KOD (Catheter, Urological), a Class II device regulated under 21 CFR 876.5130. American Pharmaseal Div. Ahsc has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 3, 1987
Date Received
November 2, 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