The following data is part of a premarket notification filed by Espe Gmbh (us) with the FDA for Modified Permagum Adhesive.
Device ID | K881838 |
510k Number | K881838 |
Device Name: | MODIFIED PERMAGUM ADHESIVE |
Classification | Material, Impression Tray, 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 | EBH |
CFR Regulation Number | 872.3670 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-05-02 |
Decision Date | 1988-07-27 |