Mui Scientific

FDA Regulatory Profile

Mui Scientific has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Mar 14, 2017

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances4Oct 4, 2026Not statedCurrent
Inspections0Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K160287Rapid Barostat Bag (RBB) Pump and CatheterMar 14, 2017
K122294PRESSURIZED INFUSION PUMPNov 1, 2012
K120524SPHINCTER OF ODDI MANOMETRIC (SOM) SYSTEMJun 21, 2012
K823701MOTILITY CATHETERSFeb 15, 1983