The following data is part of a premarket notification filed by Fisher Diagnostics with the FDA for Architect Stat Myo Immunoassay.
Device ID | K042924 |
510k Number | K042924 |
Device Name: | ARCHITECT STAT MYO IMMUNOASSAY |
Classification | Myoglobin, Antigen, Antiserum, Control |
Applicant | FISHER DIAGNOSTICS 8365 VALLEY PIKE, PO BX 307 Middletown, VA 22645 |
Contact | Josefina Infantas |
Correspondent | Josefina Infantas FISHER DIAGNOSTICS 8365 VALLEY PIKE, PO BX 307 Middletown, VA 22645 |
Product Code | DDR |
CFR Regulation Number | 866.5680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-10-22 |
Decision Date | 2005-01-24 |
Summary: | summary |