UROSURGE PERCUTANEOUS SANS (STOLLER AFFERENT NERVE STIMULATOR) DEVICE— 510(k) DEN000002
UnknownUrosurge, Inc.
FDA 510(k) clearance DEN000002 for UROSURGE PERCUTANEOUS SANS (STOLLER AFFERENT NERVE STIMULATOR) DEVICE, Unknown on 2000-02-09. Applicant: Urosurge, Inc.. Device class: 2.
Clearance details
- Applicant
- Urosurge, Inc.
- Product code
- Code NAM
- Device class
- Class 2
- Regulation
- 21 CFR 876.5310
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Post-NSE
- Location
- Coralville, IA, US
Recent devices under product code NAM
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view allAdverse events under product code NAM
product code NAM- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.