H R Pharmaceuticals, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
H R Pharmaceuticals, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AquaFlate Pre-Filled Sterile Water Syringe 10mL, EcoVue Sterile and Non-Sterile Ultrasound Gels
2
Total
2
Cleared
0
Denied
H R Pharmaceuticals, Inc. has 2 FDA 510(k) cleared medical devices. Based in York, US.
Historical record: 2 cleared submissions from 2018 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by H R Pharmaceuticals, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - H R Pharmaceuticals, Inc.
2 devices