Medical Device Manufacturer · US , Dover , DE

Altamira Therapeutics, Inc. - FDA 510(k) Cleared Devices

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

Altamira Therapeutics, Inc. has 1 FDA 510(k) cleared medical devices. Based in Dover, US.

Last cleared in 2022. Active since 2022. Primary specialty: Ear, Nose, Throat.

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

FDA 510(k) cleared devices by Altamira Therapeutics, Inc.

1 devices
1-1 of 1
Cleared Jun 24, 2022
BentrioTM Allergy Blocker
K213114 · NUP
Ear, Nose, Throat · 270d
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