RUSCH PERCUTANEOUS NEPHROSTOMY CATHETER SETS— 510(k) K011121
Substantially EquivalentRusch Intl.
FDA 510(k) clearance K011121 for RUSCH PERCUTANEOUS NEPHROSTOMY CATHETER SETS, Substantially Equivalent on 2001-11-16. Applicant: Rusch Intl.. Device class: Unclassified.
Clearance details
- Applicant
- Rusch Intl.
- Product code
- Code LJE
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Jaffrey, NH, US
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More clearances from Rusch Intl.
view allAdverse events under product code LJE
product code LJE- Death
- 6
- Total
- 6
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.