The following data is part of a premarket notification filed by Argen Precious Metals, Inc. with the FDA for Argebond 80.
Device ID | K913704 |
510k Number | K913704 |
Device Name: | ARGEBOND 80 |
Classification | Alloy, Other Noble Metal |
Applicant | ARGEN PRECIOUS METALS, INC. 8380 MIRALANI DR. San Diego, CA 92126 |
Contact | Lal Malhotra |
Correspondent | Lal Malhotra ARGEN PRECIOUS METALS, INC. 8380 MIRALANI DR. San Diego, CA 92126 |
Product Code | EJS |
CFR Regulation Number | 872.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-08-19 |
Decision Date | 1991-11-13 |