Oncolog Medical QA AB is one of 136 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Oncolog Medical QA AB - FDA 510(k) Cleared Devices
Recent clearances: PATLOG 2.0, PATLOG, PATLOG PATIENT HANDLING SYSTEM, PATLOG TOPLOG TABLE TOP, MODEL(S) 1.0, 1.0, C
2
Total
2
Cleared
0
Denied
Oncolog Medical QA AB has 2 FDA 510(k) cleared medical devices. Based in Uppsala, SE.
Historical record: 2 cleared submissions from 2009 to 2009. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Oncolog Medical QA AB Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Oncolog Medical QA AB
2 devices