The following data is part of a premarket notification filed by American Monitor Corp. with the FDA for Bio Interference Blanking Material.
Device ID | K823687 |
510k Number | K823687 |
Device Name: | BIO INTERFERENCE BLANKING MATERIAL |
Classification | Single (specified) Analyte Controls (assayed And Unassayed) |
Applicant | AMERICAN MONITOR CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JJX |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-12-07 |
Decision Date | 1983-01-07 |