Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
HLZ
2026-04-01
ODP
2026-04-01
MOD-C
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MOS
2026-04-01
GEM Flex Coil 16-L Array, 3.0T Receive Only; GEM Flex Coil 16-M Array, 3.0T Receive Only; GEM Flex Coil 16-S Array, 3.0T Receive Only
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FOZ
2026-04-01
Polywin Safety (14G x 51mm; 16G x 51mm; 18G x 64mm; 20G x 64mm; 20G x 45mm; 22G x 64mm; 22G x 45mm; 24G x 32mm; 24G x 14mm, 26G x 14mm); Polywin Safety Adva (20G x 45mm; 22G x 64mm; 22G x 45mm ; 24G x 32 mm; 24G x 14mm; 14G x 51mm; 16G x 51mm; 18G x 64mm; 20G x 64mm, 26G x 14mm)
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QIH
2026-04-01
CoLumbo C-Spine
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GEI
2026-04-01
Prana System
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HRS
2026-04-01
enHAnce PEEK Bunion System
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DXN
2026-04-01
Arm Blood Pressure Monitor Models: ARM-30C+; ARM-30M+; ARM-HA101+; ARM-3060; XS Pro; ARM-30G1; ARM-30H; Visomat double comfort; Visomat comfort 20/40 BT; ARM-3080; ARM-3081; ARM-3082; ARM-3103; ARM-3200; ARM-115; ARM-111; ARM-3102; ARM-3100; ARM-3101; SBM 15; ARM-30W; ARM-30J; ARM-30F-XL; ARM-3024-XL; ARM-3025-XL; ARM-3062-XL; 9S Pro
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EZD
2026-04-01
GentleCath Air for Men; GentleCath Glide Intermittent Catheter; GentleCath Air for Women
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NUC
2026-04-01
Hyaluronic Acid Vaginal Suppository (HA 5 mg); Hyaluronic Acid Vaginal Suppository (HA 10 mg)
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SHN
2026-04-01
Medical Imaging Calibration Feature (MICF)
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DQK
2026-04-01
Synchrony
Ver detalhes →Nenhum dispositivo correspondente.
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