510(k) K983245

POS-T-VAC (AVP-1000) by Pos-T-Vac, Inc. — Product Code LKY

K983245 is an FDA 510(k) premarket notification submitted by Pos-T-Vac, Inc. for the device "POS-T-VAC (AVP-1000)". The FDA issued a decision of Substantially Equivalent on November 2, 1998. The device falls under product code LKY (Device, External Penile Rigidity), a Class II device regulated under 21 CFR 876.5020. Pos-T-Vac, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 2, 1998
Date Received
September 16, 1998
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.