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Viratest Intl., Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K955921
A549 CELL CULTURE
February 16, 1996
K952727
MRC-5 CELL CULTURE VIAL
November 20, 1995
K931922
DIADOT(TM) VIRUS/CHLAMYDIA TRANSPORT
March 30, 1994