The following data is part of a premarket notification filed by Pos-t-vac, Inc. with the FDA for Pos-t-vac Avp-1000 & Mvp-700.
| Device ID | K960342 |
| 510k Number | K960342 |
| Device Name: | POS-T-VAC AVP-1000 & MVP-700 |
| Classification | Device, External Penile Rigidity |
| Applicant | POS-T-VAC, INC. 2550 M STREET, N.W. Washington, DC 20037 |
| Contact | Mark A Heller |
| Correspondent | Mark A Heller POS-T-VAC, INC. 2550 M STREET, N.W. Washington, DC 20037 |
| Product Code | LKY |
| CFR Regulation Number | 876.5020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-01-24 |
| Decision Date | 1996-03-01 |