The following data is part of a premarket notification filed by Immuno Concepts, Inc. with the FDA for Relisa Sm/rnp Antibody Test System.
Device ID | K955604 |
510k Number | K955604 |
Device Name: | RELISA SM/RNP ANTIBODY TEST SYSTEM |
Classification | Extractable Antinuclear Antibody, Antigen And 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 | LLL |
CFR Regulation Number | 866.5100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-12-08 |
Decision Date | 1996-04-19 |
Summary: | summary |