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Mui Scientific

FDA Regulatory Profile

Mui Scientific appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 14, 2017.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K160287Rapid Barostat Bag (RBB) Pump and CatheterMarch 14, 2017
K122294PRESSURIZED INFUSION PUMPNovember 1, 2012
K120524SPHINCTER OF ODDI MANOMETRIC (SOM) SYSTEMJune 21, 2012
K823701MOTILITY CATHETERSFebruary 15, 1983

FDA data resources