510(k) K960828
K960828 is an FDA 510(k) premarket notification submitted by Pos-T-Vac, Inc. for the device "POS-T-VAC B-10 BAND KIT". The FDA issued a decision of Substantially Equivalent on March 8, 1996. 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
- March 8, 1996
- Date Received
- February 29, 1996
- 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.