The following data is part of a premarket notification filed by Ventana Medical Systems, Inc. with the FDA for Ventana Negative Control Reagent.
Device ID | K931979 |
510k Number | K931979 |
Device Name: | VENTANA NEGATIVE CONTROL REAGENT |
Classification | Alpha-1-antitrypsin, Antigen, Antiserum, Control |
Applicant | VENTANA MEDICAL SYSTEMS, INC. 3865 N. BUSINESS CENTER DR. Tucson, AZ 85705 |
Contact | Stephen A Tillson |
Correspondent | Stephen A Tillson VENTANA MEDICAL SYSTEMS, INC. 3865 N. BUSINESS CENTER DR. Tucson, AZ 85705 |
Product Code | DEM |
CFR Regulation Number | 866.5130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-04-22 |
Decision Date | 1994-03-30 |