The following data is part of a premarket notification filed by Ventana Medical Systems, Inc. with the FDA for Ventana Anti-cd5 Primary Antibody.
Device ID | K941782 |
510k Number | K941782 |
Device Name: | VENTANA ANTI-CD5 PRIMARY ANTIBODY |
Classification | Lambda, Antigen, Antiserum, Control |
Applicant | VENTANA MEDICAL SYSTEMS, INC. 3865 N. BUSINESS CENTER DR. Tucson, AZ 85705 |
Contact | Stephen Tillson |
Correspondent | Stephen Tillson VENTANA MEDICAL SYSTEMS, INC. 3865 N. BUSINESS CENTER DR. Tucson, AZ 85705 |
Product Code | DEH |
CFR Regulation Number | 866.5550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-04-11 |
Decision Date | 1996-09-10 |
Summary: | summary |