FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
GEI
2024-08-05
MPA
2024-08-05
Midfield Light Pipe, 23ga (3269.M06-00); Midfield Light Pipe, 25ga (3269.M05-00); Midfield Light Pipe, 27ga (3269.M04-00)
View Details →
GEI
2024-08-05
CellFX Percutaneous Electrode System (SYS3000); CellFX Percutaneous Electrode, 13G (CPE013); CellFX Percutaneous Electrode, 18G (CPE018)
View Details →
LCJ
2024-08-02
MENTOR™ CPX™4 PLUS Enhance Breast Tissue Expander
View Details →
GEX
2024-08-02
Diode Laser Hair Removal System (MBT-Diode Laser)
View Details →
QDA
2024-08-02
Samsung ECG App v 1.3 (ECG)
View Details →
NKB
2024-08-02
Cortera™ Spinal Fixation System
View Details →
MBI
2024-08-02
Fixone Meniscal Repair
View Details →
IPF
2024-08-02
MYOTouch Muscle Stimulator
View Details →
LZA
2024-08-02
Powder Free Nitrile Examination Gloves (Blue), Tested for Use with Chemotherapy Drugs and Fentanyl Citrate (XS,S,M,L,XL,XXL)
View Details →
HIH
2024-08-02
Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101)
View Details →
PGY
2024-08-02
Coronis OneLook
View Details →No matching devices.
Page 558 of 2738