Techbopulm, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Techbopulm, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: STS
1
Total
1
Cleared
0
Denied
Techbopulm, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Yad Benyamin, IL.
Latest FDA clearance: Sep 2024. Active since 2024. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Techbopulm, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by ProMedoss, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Techbopulm, Ltd.
1 devices