# K990006: Erco-Vac -C

- Pathway: 510(k) (Traditional)
- Applicant: Ercons, Inc.
- Decided: Feb 24, 1999 after 51 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
Longest line of descent: 2 generations back to K841257 (1984). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K841257: Sta-Potent System, Nu-Potent (1984) Summary page 1.
- K901223: Vacuum Erection Device (Ved), Mission Pharmacal Co. (1990) Summary page 1.
- K960828: Pos-T-Vac B-10 Band Kit, Pos-T-Vac, Inc. (1996) Summary page 1.
- K981357: Erco-Vac, Ercons, Inc. (1998) Summary page 1.

## Indications for use
Erco-Vac™ -C is used to create an erection in men with erectile dysfunction and for augmenting of male potency. Erco-Vac™ —C can be used for patients with following conditions: Diabetes Venous leakage Prostatectomy Hypertension Psychogenic condition Impotence due to radiation therapy Spinal cord injury

Source page: https://510kreport.com/device/K990006
Methodology: https://510kreport.com/methodology