The following data is part of a premarket notification filed by Ventana Medical Systems, Inc. with the FDA for Ventanna Anti-desmin Primary Antibody.
Device ID | K941516 |
510k Number | K941516 |
Device Name: | VENTANNA ANTI-DESMIN PRIMARY ANTIBODY |
Classification | Lambda, Antigen, Antiserum, Control |
Applicant | VENTANA MEDICAL SYSTEMS, INC. 3865 N. BUSINESS CENTER DR. Tucson, AZ 85705 |
Contact | Steve Tillson |
Correspondent | Steve 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 | 1994-03-29 |
Decision Date | 1997-02-10 |
Summary: | summary |