S.L.P. , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
S.L.P. , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: OxSAT 100
5
Total
5
Cleared
0
Denied
S.L.P. , Ltd. has 5 FDA 510(k) cleared medical devices. Based in Tel-Aviv, IL.
Historical record: 5 cleared submissions from 2004 to 2020. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by S.L.P. , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by S.L.P. Ltd. C/O Promedic, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - S.L.P. , Ltd.
5 devices