Dynarad Corp.

FDA Regulatory Profile

Dynarad Corp. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Feb 10, 2000.

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K000052X-RAY MONOBLOCK, MONOBLOCK XRS-60-330Feb 10, 2000
K981267FACTS MONOBLOCKMay 6, 1998
K973833CONTROL, X-RAY DIAGNOSTIC, GENERATOR, HIGH VOLTAGE, ASSEMBLY, TUBE HOUSING DIAGNOSTIC, BEAM LIMITINGDec 30, 1997
K932356NOVA XM2Feb 8, 1995
K941363PHANTOMJul 20, 1994
K932353HF-110AJan 31, 1994
K9323559150A, 1100FAug 3, 1993
K9323549170, 1170Jul 23, 1993
K931725ALPHA IIJul 14, 1993