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FDA 510(k) Applications Submitted by DYNARAD CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K981267
04/07/1998
FACTS MONOBLOCK
DYNARAD CORP.
K973833
10/07/1997
CONTROL, X-RAY DIAGNOSTIC, GENERATOR, HIGH VOLTAGE, ASSEMBLY, TUBE HOUSING DIAGNOSTIC, BEAM LIMITING DEVICE, MANUAL
DYNARAD CORP.
K000052
01/07/2000
X-RAY MONOBLOCK, MONOBLOCK XRS-60-330
DYNARAD CORP.
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