FDA 510(k) Applications Submitted by DENTAL MANUFACTURING S.P.A
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K013824 | 11/19/2001 | ACRY PLUS, ACRY LUX, ACRY LUX V, ACRY ROCK, ACRY ROCK V AND Z-TONE PREFORMED PLASTIC DENTURE TEETH | DENTAL MANUFACTURING S.P.A |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact