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Hakki Medical Technologies, Inc.

FDA Regulatory Profile

Hakki Medical Technologies, Inc. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 21, 2020.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K191512LotusCatheter (Lotus No Balloon Catheter)May 21, 2020
K101900HAKKI URINARY CATHETER; SIZE 14, 16, 18, 20, 22, 24, 26 FRENCHFebruary 7, 2011

FDA data resources