FDA 510(k) Applications Submitted by BETSY SOARES-MADDOX

FDA 510(k) Number Submission Date Device Name Applicant
K980853 03/05/1998 CEDIA DAU MULTI-DRUG CALIBRATORS BOEHRINGER MANNHEIM CORP.
K961462 04/17/1996 CEDIA THEOPHYLLINE ASSAY BOEHRINGER MANNHEIM CORP.
K961489 04/18/1996 ELECSYS FT4 ASSAY BOEHRINGER MANNHEIM CORP.
K961491 04/18/1996 ELECSYS TSH ASSAY BOEHRINGER MANNHEIM CORP.
K962734 07/15/1996 CEDIA DAU BENZODIAZEPINE ASSAY BOEHRINGER MANNHEIM CORP.
K962795 07/18/1996 CEDIA DAU OPIATE 2K ASSAY BOEHRINGER MANNHEIM CORP.
K963191 08/15/1996 CEDIA ANTIBIOTIC TDM MULTI-CALS BOEHRINGER MANNHEIM CORP.
K964693 11/22/1996 ELECSYS FSH ASSAY BOEHRINGER MANNHEIM CORP.
K964694 11/22/1996 ELECSYS LH ASSAY BOEHRINGER MANNHEIM CORP.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact