MODEL P8400 HEMOSTATIX THERMAL SCALPEL SYSTEM— 510(k) K091107
Substantially EquivalentHemostatix Medical Technologies, LLC
FDA 510(k) clearance K091107 for MODEL P8400 HEMOSTATIX THERMAL SCALPEL SYSTEM, Substantially Equivalent on 2009-05-01. Applicant: Hemostatix Medical Technologies, LLC.
Clearance details
- Applicant
- Hemostatix Medical Technologies, LLC
- Product code
- Code GEI
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bartlett, TN, US
Adverse events under product code GEI
product code GEI- Death
- 133
- Injury
- 7,585
- Malfunction
- 35,808
- Other
- 44
- Total
- 43,570
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.