Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Dynarad Corp.

FDA 510(k) & PMA Approved Devices — 9 products

Total Devices9
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K000052 X-RAY MONOBLOCK, MONOBLOCK XRS-60-330ITY2000-02-10 View
510(k) K981267 FACTS MONOBLOCKIZX1998-05-06 View
510(k) K973833 CONTROL, X-RAY DIAGNOSTIC, GENERATOR, HIGH VOLTAGE, ASSEMBLY, TUBE HOUSING DIAGNOSTIC, BEAM LIMITING DEVICE, MANUALIZL1997-12-30 View
510(k) K932356 NOVA XM2IZH1995-02-08 View
510(k) K941363 PHANTOMIZL1994-07-20 View
510(k) K932353 HF-110AIZL1994-01-31 View
510(k) K932355 9150A, 1100FIZL1993-08-03 View
510(k) K932354 9170, 1170IZL1993-07-23 View
510(k) K931725 ALPHA IIEHD1993-07-14 View
↑