Meddiff Technologies Pvt. , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Meddiff Technologies Pvt. , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: InstaRISPACS / InstaZFP / InstaMobi v5.0
2
Total
2
Cleared
0
Denied
Meddiff Technologies Pvt. , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Denton, US.
Historical record: 2 cleared submissions from 2012 to 2019. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Meddiff Technologies Pvt. , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by O Tech, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Meddiff Technologies Pvt. , Ltd.
2 devices