The following data is part of a premarket notification filed by Ab Ardent with the FDA for Amalcap Plus.
Device ID | K982456 |
510k Number | K982456 |
Device Name: | AMALCAP PLUS |
Classification | Alloy, Amalgam |
Applicant | AB ARDENT 54 RIVERVIEW AVE. Tonawanda, NY 14150 -5260 |
Contact | Clyde E Ingersoll |
Correspondent | Clyde E Ingersoll AB ARDENT 54 RIVERVIEW AVE. Tonawanda, NY 14150 -5260 |
Product Code | EJJ |
CFR Regulation Number | 872.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-07-15 |
Decision Date | 1998-08-24 |