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Bioware Products

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K810144ALK-PHOS BIOPAK GELFebruary 2, 1981
K802299K/K (ASMA/ANA) UNIVERSAL BIOPAKJanuary 29, 1981
K802308T/K (ATA/AMA) UNIVERSAL BIOPAKDecember 1, 1980
K802276FTA-ABS BIOPAKOctober 23, 1980