FDA applicant
National Rehab Hospital
FDA records 1 decision for National Rehab Hospital (Washington, DC) in 1997: 1 510(k) clearance. All are in product code LNL (Stimulator, Electrical For Sperm Collection). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided National Rehab Hospital’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for National Rehab Hospital since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like National Rehab Hospital’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report