MODIFICATION TO PANAVIA F— 510(k) K002322
Substantially EquivalentKuraray America, Inc.
FDA 510(k) clearance K002322 for MODIFICATION TO PANAVIA F, Substantially Equivalent on 2000-09-18. Applicant: Kuraray America, Inc..
Clearance details
- Applicant
- Kuraray America, Inc.
- Product code
- Code EMA
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.