The following data is part of a premarket notification filed by E&d Dental Manufacturing Co. with the FDA for Eugenol Usp.
Device ID | K862745 |
510k Number | K862745 |
Device Name: | EUGENOL USP |
Classification | Zinc Oxide Eugenol |
Applicant | E&D DENTAL MANUFACTURING CO. 6 HOFFMAN PLACE HILLSIDE, NJ 07205 |
Contact | ED SPEHAR |
Correspondent | ED SPEHAR E&D DENTAL MANUFACTURING CO. 6 HOFFMAN PLACE HILLSIDE, NJ 07205 |
Product Code | EMB |
CFR Regulation Number | 872.3275 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-07-21 |
Decision Date | 1986-07-31 |