Diesse Diagnostica Senese S.P.A. is one of 23826 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diesse Diagnostica Senese S.P.A. - FDA 510(k) Cleared Devices
Recent clearances: COPROSET SALMONELLA AND SHIGELLA, URISET PRESERVATIVE TUBES AND SWAB SET GENERAL USE, ENZY-WELL SYPHILIS IGG, MODEL 91106
2
Total
2
Cleared
0
Denied
Diesse Diagnostica Senese S.P.A. has 2 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 2 cleared submissions from 2006 to 2007. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Diesse Diagnostica Senese S.P.A. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Diesse Diagnostica Senese S.P.A.
2 devices