PLAKOF— 510(k) K890910
Substantially EquivalentXimex, Ltd.
FDA 510(k) clearance K890910 for PLAKOF, Substantially Equivalent on 1989-03-16. Applicant: Ximex, Ltd.. Device class: 1.
Clearance details
- Applicant
- Ximex, Ltd.
- Product code
- Code JET
- Device class
- Class 1
- Regulation
- 21 CFR 872.6650
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- England Sw13 9nt, GB
Recent devices under product code JET
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