DISPERSALLOY-DISPERSED PHASE ALLOY SELF-— 510(k) K802967
Substantially EquivalentJohnson & Johnson Professionals, Inc.
FDA 510(k) clearance K802967 for DISPERSALLOY-DISPERSED PHASE ALLOY SELF-, Substantially Equivalent on 1980-12-30. Applicant: Johnson & Johnson Professionals, Inc.. Device class: 1.
Clearance details
- Applicant
- Johnson & Johnson Professionals, Inc.
- Product code
- Code DZS
- Device class
- Class 1
- Regulation
- 21 CFR 872.3110
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Raynham, MA, US
Recent devices under product code DZS
view allMore clearances from Johnson & Johnson Professionals, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.