The following data is part of a premarket notification filed by Instrumentation Laboratory Co. with the FDA for Quantex Myoglobin.
Device ID | K042982 |
510k Number | K042982 |
Device Name: | QUANTEX MYOGLOBIN |
Classification | Myoglobin, Antigen, Antiserum, Control |
Applicant | INSTRUMENTATION LABORATORY CO. 180 HARTWELL ROAD Bedford, MA 01730 |
Contact | Carol Marble |
Correspondent | Carol Marble INSTRUMENTATION LABORATORY CO. 180 HARTWELL ROAD Bedford, MA 01730 |
Product Code | DDR |
Subsequent Product Code | JIT |
Subsequent Product Code | JJX |
CFR Regulation Number | 866.5680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-10-29 |
Decision Date | 2004-12-22 |
Summary: | summary |