CALCIJECT— 510(k) K001050
Substantially EquivalentCentrix, Inc.
FDA 510(k) clearance K001050 for CALCIJECT, Substantially Equivalent on 2000-07-21. Applicant: Centrix, Inc.. Device class: 2.
Clearance details
- Applicant
- Centrix, Inc.
- Product code
- Code EJK
- Device class
- Class 2
- Regulation
- 21 CFR 872.3250
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shelton, CT, US
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