The following data is part of a premarket notification filed by J.s. Medical Assoc. with the FDA for Accutex Im Rbc Test.
Device ID | K924037 |
510k Number | K924037 |
Device Name: | ACCUTEX IM RBC TEST |
Classification | System, Test, Infectious Mononucleosis |
Applicant | J.S. MEDICAL ASSOC. 19 STRATHMORE RD. Natick, MA 01760 |
Contact | Richard Davis |
Correspondent | Richard Davis J.S. MEDICAL ASSOC. 19 STRATHMORE RD. Natick, MA 01760 |
Product Code | KTN |
CFR Regulation Number | 866.5640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-08-11 |
Decision Date | 1992-11-02 |