Cytovale, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cytovale, Inc. - FDA 510(k) Cleared Devices
Recent clearances: IntelliSep Test, IntelliSep Test (CV-ICG-048), IntelliSep test
3
Total
3
Cleared
0
Denied
Cytovale, Inc. has 3 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Latest FDA clearance: Nov 2025. Active since 2022. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Cytovale, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Cytovale, Inc.
3 devices