# K960342: Pos-T-Vac Avp-1000 & MVP-700

- Pathway: 510(k) (Traditional)
- Applicant: Pos-T-Vac, Inc.
- Decided: Mar 1, 1996 after 37 days
- Product code: LKY (Device, External Penile Rigidity)
- Device class: 2
- Regulation: 21 CFR 876.5020
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K981357: Erco-Vac (1998), 1 descendant of its own
- K990006: Erco-Vac -C (1999), 0 descendants of its own
- K972537: Erco-Vac (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K960342
Methodology: https://510kreport.com/methodology