510(k) K963328

AMS AMBICOR PENILE PROSTHESIS by American Medical Systems, Inc. — Product Code FAE

K963328 is an FDA 510(k) premarket notification submitted by American Medical Systems, Inc. for the device "AMS AMBICOR PENILE PROSTHESIS". The FDA issued a decision of Substantially Equivalent on December 4, 1996. The device falls under product code FAE (Prosthesis, Penile), a Class II device regulated under 21 CFR 876.3630. American Medical Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 4, 1996
Date Received
August 23, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Penile
Device Class
Class II
Regulation Number
876.3630
Review Panel
GU
Submission Type