The following data is part of a premarket notification filed by Cepheid with the FDA for Xpert Mrsa/sa Blood Culture Assay.
Device ID | K082140 |
510k Number | K082140 |
Device Name: | XPERT MRSA/SA BLOOD CULTURE ASSAY |
Classification | System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococcus Aureus, Direct Specimen |
Applicant | CEPHEID 904 CARIBBEAN DRIVE Sunnyvale, CA 94089 -1189 |
Contact | Russel K Enns |
Correspondent | Russel K Enns CEPHEID 904 CARIBBEAN DRIVE Sunnyvale, CA 94089 -1189 |
Product Code | NQX |
CFR Regulation Number | 866.1640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-07-30 |
Decision Date | 2008-09-29 |
Summary: | summary |