# K962379: Seager Electroejaculator

- Pathway: 510(k) (Traditional)
- Applicant: National Rehab Hospital
- Decided: Sep 18, 1997 after 455 days
- Product code: LNL (Stimulator, Electrical For Sperm Collection)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) A. Stiebel’s electroejaculation equipment: named in the summary without a submission number

## Indications for use
The Seager Electroejaculator (EE) is intended to induce seminal emission in patients for whom prior or present illness precludes their ability to spontaneously ejaculate. The EE device is indicated for use in neurologically impaired males over the age of 18 years of age and who are anejaculatory due to the following conditions: Spinal Cord Injury (paralysis) Retroperitoneal Lymph Node Dissection (RPLND) [surgical therapy post testicular cancer] Idiopathic (neuropsychosis/psychogenic) Diabetes Spina Bifida Pelvic Surgery Complications Multiple Sclerosis (MS) Neurological Impairments

Source page: https://510kreport.com/device/K962379
Methodology: https://510kreport.com/methodology