Techbopulm, Ltd. - FDA 510(k) Cleared Devices
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.
1 devices