FDA 510(k) Applications Submitted by RAY E MORROW
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960480 | 02/02/1996 | IN-CERAM SPINELL KIT FOR CELAV MODEL V56-001/E63013 | VIDENT |
| K961434 | 04/15/1996 | VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEM | VIDENT |
| K962333 | 06/17/1996 | V.R.S. DENTURE RESIN MATERIAL | VIDENT |
| K982664 | 07/31/1998 | VITA TITANIUM PORCELAIN | VIDENT |
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