SHARPE ENDODISSECTOR— 510(k) K921888
Substantially EquivalentPaladin Medical, Inc.
FDA 510(k) clearance K921888 for SHARPE ENDODISSECTOR, Substantially Equivalent on 1992-10-20. Applicant: Paladin Medical, Inc..
Clearance details
- Applicant
- Paladin Medical, Inc.
- Product code
- Code HET
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Stillwater, MN, US
Adverse events under product code HET
product code HET- Malfunction
- 10,504
- Total
- 10,504
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.