LEONARD ARM - SUPPORT ARM - ENDOSCOPIC ACCESSORY— 510(k) K951854
Substantially EquivalentLeonard Medical, Inc.
FDA 510(k) clearance K951854 for LEONARD ARM - SUPPORT ARM - ENDOSCOPIC ACCESSORY, Substantially Equivalent on 1995-06-21. Applicant: Leonard Medical, Inc..
Clearance details
- Applicant
- Leonard Medical, Inc.
- Product code
- Code FQO
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Huntingdon Valley, PA, US
Adverse events under product code FQO
product code FQO- Death
- 6
- Injury
- 145
- Malfunction
- 685
- Total
- 836
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.