SMDIA-1000— 510(k) K101953
Substantially EquivalentSouthmedic, Inc.
FDA 510(k) clearance K101953 for SMDIA-1000, Substantially Equivalent on 2011-01-07. Applicant: Southmedic, Inc..
Clearance details
- Applicant
- Southmedic, Inc.
- Product code
- Code CAF
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bonita Springs, FL, US
Adverse events under product code CAF
product code CAF- Death
- 22
- Injury
- 125
- Malfunction
- 613
- Other
- 11
- Total
- 771
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.