Medical Device Manufacturer · US , Los Angeles , CA

Dr. Harold Katz, LLC (Dba Therabreath - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2018
1
Total
1
Cleared
0
Denied

Dr. Harold Katz, LLC (Dba Therabreath has 1 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Dr. Harold Katz, LLC (Dba Therabreath Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Dr. Harold Katz, LLC (Dba Therabreath

1 devices
1-1 of 1
Cleared Mar 16, 2018
TheraBreath Dry Mouth Oral Rinse, TheraBreath Dry Mouth Lozenges
K171542 · LFD
Dental · 294d
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