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Pb Diagnostics, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K925703
OPUS SEROLOGY CONTROLS
April 8, 1993
K921523
OPUS(R) TOXO-G TEST SYSTEM
September 14, 1992
K915870
OPUS RUBELLA TEST SYSTEM
March 23, 1992
K913080
OPUS(R) ANTI CMV-M
October 28, 1991