Device Classification Name |
System, Test, Automated, Antimicrobial Susceptibility, Short Incubation
|
510(k) Number |
K223481 |
Device Name |
VITEK® 2 Streptococcus Tetracycline (<=0.25 - >=16 µg/mL) |
Applicant |
bioMerieux, Inc |
595 Anglum Rd. |
Hazelwood,
MO
63042
|
|
Applicant Contact |
Jared Bronson |
Correspondent |
bioMerieux, Inc |
595 Anglum Rd. |
Hazelwood,
MO
63042
|
|
Correspondent Contact |
Jared Bronson |
Regulation Number | 866.1645
|
Classification Product Code |
|
Date Received | 11/18/2022 |
Decision Date | 02/03/2023 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Microbiology
|
510k Review Panel |
Microbiology
|
Summary |
Summary
|
FDA Review |
Decision Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|