Breathe Me, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Breathe Me, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Peak.me
1
Total
1
Cleared
0
Denied
Breathe Me, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Ra'Anana, IL.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Breathe Me, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qsite as regulatory consultant.
FDA 510(k) Regulatory Record - Breathe Me, Ltd.
1 devices