The following data is part of a premarket notification filed by Bayer Corp. with the FDA for N-acetylprocainamide Assay For The Bayer Immuno 1 System.
Device ID | K971713 |
510k Number | K971713 |
Device Name: | N-ACETYLPROCAINAMIDE ASSAY FOR THE BAYER IMMUNO 1 SYSTEM |
Classification | Enzyme Immunoassay, N-acetylprocainamide |
Applicant | BAYER CORP. 511 BENEDICT AVE. Tarrytown, NY 10591 -5097 |
Contact | Gabriel J Muraca, Jr. |
Correspondent | Gabriel J Muraca, Jr. BAYER CORP. 511 BENEDICT AVE. Tarrytown, NY 10591 -5097 |
Product Code | LAN |
CFR Regulation Number | 862.3320 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-05-09 |
Decision Date | 1997-06-11 |
Summary: | summary |