The following data is part of a premarket notification filed by Ortho Diagnostic Systems, Inc. with the FDA for Ortho-mune Okt 4 (cd4) Monoclonal Antibody Murine.
Device ID | K932531 |
510k Number | K932531 |
Device Name: | ORTHO-MUNE OKT 4 (CD4) MONOCLONAL ANTIBODY MURINE |
Classification | Counter, Differential Cell |
Applicant | ORTHO DIAGNOSTIC SYSTEMS, INC. 1001 U.S. HIGHWAY 202 P.O. BOX 350 Raritan, NJ 08869 -0606 |
Contact | Patrick Roche |
Correspondent | Patrick Roche ORTHO DIAGNOSTIC SYSTEMS, INC. 1001 U.S. HIGHWAY 202 P.O. BOX 350 Raritan, NJ 08869 -0606 |
Product Code | GKZ |
CFR Regulation Number | 864.5220 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-05-18 |
Decision Date | 1995-04-26 |