Tampro, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tampro, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Sequel Tampon with Plastic Applicator
1
Total
1
Cleared
0
Denied
Tampro, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Fransisco, US.
Last cleared in 2023. Active since 2023. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Tampro, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory and Technical Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Tampro, Inc.
1 devices