510(k) K900774

DACOMED NEGATIVE PRESSURE ERECTION DEVICE by Dacomed Corp. — Product Code LKY

K900774 is an FDA 510(k) premarket notification submitted by Dacomed Corp. for the device "DACOMED NEGATIVE PRESSURE ERECTION DEVICE". The FDA issued a decision of Substantially Equivalent on May 4, 1990. The device falls under product code LKY (Device, External Penile Rigidity), a Class II device regulated under 21 CFR 876.5020. Dacomed Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 4, 1990
Date Received
February 20, 1990
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.