The following data is part of a premarket notification filed by Espe Gmbh (us) with the FDA for Espe Ketac-bond.
Device ID | K844845 |
510k Number | K844845 |
Device Name: | ESPE KETAC-BOND |
Classification | Coating, Filling Material, 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 | EBD |
CFR Regulation Number | 872.3310 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-12-13 |
Decision Date | 1985-08-19 |