Dr. Harold Katz, LLC (Dba Therabreath is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dr. Harold Katz, LLC (Dba Therabreath - FDA 510(k) Cleared Devices
Recent clearances: TheraBreath Dry Mouth Oral Rinse, TheraBreath Dry Mouth Lozenges
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.
510(k) submissions have been managed by Clinical Research Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Dr. Harold Katz, LLC (Dba Therabreath
1 devices