The following data is part of a premarket notification filed by Instrumentation Laboratory Co. with the FDA for Il Test Antithrombin.
Device ID | K980499 |
510k Number | K980499 |
Device Name: | IL TEST ANTITHROMBIN |
Classification | Antithrombin Iii Quantitation |
Applicant | INSTRUMENTATION LABORATORY CO. 113 HARTWELL AVE. Lexington, MA 02173 |
Contact | Carol Marble |
Correspondent | Carol Marble INSTRUMENTATION LABORATORY CO. 113 HARTWELL AVE. Lexington, MA 02173 |
Product Code | JBQ |
CFR Regulation Number | 864.7060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-02-09 |
Decision Date | 1998-04-02 |
Summary: | summary |