Medical Device Manufacturer · CA , Toronto

Bresotec, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022
1
Total
1
Cleared
0
Denied

Bresotec, Inc. has 1 FDA 510(k) cleared medical devices. Based in Toronto, CA.

Last cleared in 2022. Active since 2022. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Bresotec, Inc. Filter by specialty or product code using the sidebar.

1 device has linked clinical trial registered on ClinicalTrials.gov.

FDA 510(k) Regulatory Record - Bresotec, Inc.
1 devices
1-1 of 1
Cleared CT Dec 21, 2022
BresoDX1
K220012 · MNR
Anesthesiology · 351d
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