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Diversified P.A.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K820571XENAMATIC SERIES OF XENON REBREATH DEVMarch 31, 1982
K812613VIDICAM 200December 8, 1981