SCLEROTHERAPY NEEDLE— 510(k) K914496
Substantially EquivalentSurgitek Medical Engineering Corp.
FDA 510(k) clearance K914496 for SCLEROTHERAPY NEEDLE, Substantially Equivalent on 1991-12-05. Applicant: Surgitek Medical Engineering Corp..
Clearance details
- Applicant
- Surgitek Medical Engineering Corp.
- Product code
- Code FBK
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Racine, WI, US
Adverse events under product code FBK
product code FBK- 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.