510(k) K974173

ERECAID SYSTEM/STAY EREC SYSTEM by Imagyn Medical Technologies, Inc. — Product Code LKY

K974173 is an FDA 510(k) premarket notification submitted by Imagyn Medical Technologies, Inc. for the device "ERECAID SYSTEM/STAY EREC SYSTEM". The FDA issued a decision of Substantially Equivalent on February 25, 1998. The device falls under product code LKY (Device, External Penile Rigidity), a Class II device regulated under 21 CFR 876.5020. Imagyn Medical Technologies, Inc. has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 25, 1998
Date Received
November 5, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, External Penile Rigidity
Device Class
Class II
Regulation Number
876.5020
Review Panel
GU
Submission Type

Intended to create or maintain sufficient penile rigidity for sexual intercourse. These include vacuum pumps, constriction rings, and penile splints, which are mechanical, powered or pneumatic devices.