510(k) K832043

SURGIKEK PENILE PROSTHESIS TAIL EXTEND by Medical Engineering Corp. — Product Code FAE

K832043 is an FDA 510(k) premarket notification submitted by Medical Engineering Corp. for the device "SURGIKEK PENILE PROSTHESIS TAIL EXTEND". The FDA issued a decision of Substantially Equivalent on October 20, 1983. The device falls under product code FAE (Prosthesis, Penile), a Class II device regulated under 21 CFR 876.3630. Medical Engineering Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 20, 1983
Date Received
June 24, 1983
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