OLBERT CATHETER SYSTEM— 510(k) K833616
Substantially EquivalentMeadox Medicals, Div. Boston Scientific Corp.
FDA 510(k) clearance K833616 for OLBERT CATHETER SYSTEM, Substantially Equivalent on 1983-12-26. Applicant: Meadox Medicals, Div. Boston Scientific Corp..
Clearance details
- Applicant
- Meadox Medicals, Div. Boston Scientific Corp.
- Product code
- Code LIT
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Adverse events under product code LIT
product code LIT- Death
- 27
- Injury
- 1,256
- Malfunction
- 12,127
- Total
- 13,410
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.