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Suzhou Leapmed Healthcare Corporation

FDA Regulatory Profile

Suzhou Leapmed Healthcare Corporation 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 July 6, 2022.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K212822Disposable Coaxial Biopsy NeedleJuly 6, 2022
K212820Disposable Semi Automatic Biopsy InstrumentJuly 6, 2022
K212819Disposable Biopsy Refill NeedleJuly 6, 2022
K212284Disposable Automatic Core Biopsy InstrumentNovember 10, 2021

FDA data resources