KGW
2026-02-23
FDA 510(k) 許可
由 MedTracker 追蹤的 510(k) 許可裝置
KLE
2026-02-23
VITA VMLC Primer
查看詳情 →
FDT
2026-02-22
Single Use Distal Cover MAJ-2315 (MAJ-2315)
查看詳情 →
FDI
2026-02-21
Advanced Tissue Resection Device
查看詳情 →
OWB
2026-02-20
CARA System
查看詳情 →
MQL
2026-02-20
CaseBio™ Culture w/HSA (CMH5); CaseBio™ Handling w/HSA (WHH5)
查看詳情 →
FMK
2026-02-20
Safety Heel Lancet
查看詳情 →
OBP
2026-02-20
SPRY TMS Therapy System (0550)
查看詳情 →
HRS
2026-02-20
KLS Martin Pure Pectus System
查看詳情 →
不適用
2026-02-20
Xpert Hemorrhagic Fever
查看詳情 →
HRS
2026-02-20
KLS Martin Ixos System
查看詳情 →
DQK
2026-02-20
CARTO™ 3 EP Navigation System V8.4
查看詳情 →沒有符合的裝置。
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