SWAN VALLEY MEDICAL TRANURETHRAL SUPRAPUBIC ENDO-CYSTOSTOMY (T-SPEC) SURGICAL SYSTEM
Oct 2012
283d
Swan Valley Medical, Incorporated
1
Total
1
Cleared
0
Denied
Swan Valley Medical, Incorporated — FDA 510(k) Submissions
Swan Valley Medical, Incorporated has submitted 1 FDA 510(k) premarket notifications since 2012, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Catheter, Suprapubic (and Accessories) . Use the specialty filter in the sidebar to narrow results.
1 devices