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Mui Scientific
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K160287
Rapid Barostat Bag (RBB) Pump and Catheter
March 14, 2017
K122294
PRESSURIZED INFUSION PUMP
November 1, 2012
K120524
SPHINCTER OF ODDI MANOMETRIC (SOM) SYSTEM
June 21, 2012
K823701
MOTILITY CATHETERS
February 15, 1983