Specific Diagnostics, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Specific Diagnostics, LLC - FDA 510(k) Cleared Devices
Recent clearances: VITEK REVEAL GN AST Assay and VITEK REVEAL AST System
1
Total
1
Cleared
0
Denied
Specific Diagnostics, LLC has 1 FDA 510(k) cleared medical devices. Based in San Jose, US.
Latest FDA clearance: Jun 2024. Active since 2024. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Specific Diagnostics, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MDC Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Specific Diagnostics, LLC
1 devices