The following data is part of a premarket notification filed by Microgenics Corp. with the FDA for Cedia Vancomycin Assay.
Device ID | K032811 |
510k Number | K032811 |
Device Name: | CEDIA VANCOMYCIN ASSAY |
Classification | Radioimmunoassay, Vancomycin |
Applicant | MICROGENICS CORP. 46360 FREMONT BLVD. Fremont, CA 94538 |
Contact | David Casal |
Correspondent | David Casal MICROGENICS CORP. 46360 FREMONT BLVD. Fremont, CA 94538 |
Product Code | LEH |
CFR Regulation Number | 862.3950 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-09-09 |
Decision Date | 2003-11-24 |
Summary: | summary |