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The Rupp & Bowman Co.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K880973
MICROLYTE 7
September 7, 1988
K882081
SPECIFIC CHEMISTRY ANALYZER
July 1, 1988
K880242
KONE CALCIUM TEST
March 15, 1988