The following data is part of a premarket notification filed by Ivoclar Usa, Inc. with the FDA for Procad.
Device ID | K980986 |
510k Number | K980986 |
Device Name: | PROCAD |
Classification | Powder, Porcelain |
Applicant | IVOCLAR USA, INC. 175 PINEVIEW DR. Amherst, NY 14150 |
Contact | Peter P Mancuso |
Correspondent | Peter P Mancuso IVOCLAR USA, INC. 175 PINEVIEW DR. Amherst, NY 14150 |
Product Code | EIH |
CFR Regulation Number | 872.6660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-03-17 |
Decision Date | 1998-05-11 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PROCAD 76300795 not registered Dead/Abandoned |
PRINTRAK INTERNATIONAL, INC. 2001-08-15 |
PROCAD 75503722 2448128 Dead/Cancelled |
Ivoclar Vivadent, Inc. 1998-06-18 |
PROCAD 73798734 1574049 Dead/Cancelled |
PROFESSIONAL CAD SERVICES, INC. 1989-05-08 |
PROCAD 73592437 not registered Dead/Abandoned |
PROCAD SYSTEMS, INC. 1986-04-09 |
PROCAD 73579539 not registered Dead/Abandoned |
TEKSOFT, INC. 1986-01-27 |
PROCAD 73573153 not registered Dead/Abandoned |
XEROX CORPORATION 1985-12-12 |