KMT2A Breakapart FISH Probe Kit PDx (CDA-LPH013)
Sep 2025
301d
Cytocell Limited
1
Total
0
Cleared
1
Denied
Cytocell Limited — FDA 510(k) Submissions
Cytocell Limited has submitted 1 FDA 510(k) premarket notifications since 2025, of which 0 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Revumenib Eligibility Detection System . Use the specialty filter in the sidebar to narrow results.
1 devices