BISCOVER LV— 510(k) K043168
Substantially EquivalentBisco, Inc.
FDA 510(k) clearance K043168 for BISCOVER LV, Substantially Equivalent on 2005-02-01. Applicant: Bisco, Inc.. Device class: 2.
Clearance details
- Applicant
- Bisco, Inc.
- Product code
- Code EBD
- Device class
- Class 2
- Regulation
- 21 CFR 872.3310
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Schaumburg, IL, US
Recent devices under product code EBD
view allMore clearances from Bisco, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.