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Intuit Medical Products, LLC

FDA Regulatory Profile

Intuit Medical Products, LLC appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 3, 2020.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K181546Dillard Nasal Balloon CatheterJanuary 3, 2020
K153484Dillard Airway Dilatation SystemJuly 27, 2016
K143738DSS Sinusplasty Balloon CatheterAugust 27, 2015

FDA data resources