The following data is part of a premarket notification filed by Espe Gmbh (us) with the FDA for Pertac-hybrid.
Device ID | K900510 |
510k Number | K900510 |
Device Name: | PERTAC-HYBRID |
Classification | Material, Tooth Shade, Resin |
Applicant | ESPE GMBH (US) 200 LAKE AVENUE (#205) Lake Worth, FL 33460 |
Contact | Harold A Opotow |
Correspondent | Harold A Opotow ESPE GMBH (US) 200 LAKE AVENUE (#205) Lake Worth, FL 33460 |
Product Code | EBF |
CFR Regulation Number | 872.3690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-02-02 |
Decision Date | 1990-08-09 |