RABEA DEVICE, MODEL PXXXXXX— 510(k) K990345
UnknownSignus Medizintechnik GmbH
FDA 510(k) clearance K990345 for RABEA DEVICE, MODEL PXXXXXX, Unknown on 1999-07-30. Applicant: Signus Medizintechnik GmbH.
Clearance details
- Applicant
- Signus Medizintechnik GmbH
- Product code
- Code JDK
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Shorewood, MN, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.