The following data is part of a premarket notification filed by Metalor Dental Usa Corp. with the FDA for Aurofluid M, Alloy No. 5315.
Device ID | K993475 |
510k Number | K993475 |
Device Name: | AUROFLUID M, ALLOY NO. 5315 |
Classification | Alloy, Other Noble Metal |
Applicant | METALOR DENTAL USA CORP. 255 JOHN L. DIETSCH BLVD. North Attleborough, MA 02761 |
Contact | Kenneth A Putney |
Correspondent | Kenneth A Putney METALOR DENTAL USA CORP. 255 JOHN L. DIETSCH BLVD. North Attleborough, MA 02761 |
Product Code | EJS |
CFR Regulation Number | 872.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-10-14 |
Decision Date | 1999-12-09 |