The following data is part of a premarket notification filed by Immuno Concepts, Inc. with the FDA for Hep-2000 Fluorescent Ana-ro Test System.
Device ID | K972145 |
510k Number | K972145 |
Device Name: | HEP-2000 FLUORESCENT ANA-RO TEST SYSTEM |
Classification | Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control |
Applicant | IMMUNO CONCEPTS, INC. 9779 BUSINESS PARK DR. SUITE D Sacramento, CA 95827 |
Contact | Eric S Hoy |
Correspondent | Eric S Hoy IMMUNO CONCEPTS, INC. 9779 BUSINESS PARK DR. SUITE D Sacramento, CA 95827 |
Product Code | DHN |
CFR Regulation Number | 866.5100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-06-06 |
Decision Date | 1998-02-24 |
Summary: | summary |