FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
DSI
1980-11-26
DOR
1980-11-26
PERICARDIOCENTESIS KIT
View Details →
GYB
1980-11-26
UCA CREAM PRODUCT REFORMULATION
View Details →
FJK
1980-11-25
ARTERIOVENOUS BLOOD TUBING SETS
View Details →
DZM
1980-11-24
MONOJECT ROOT CANAL FILLING MAT. NEEDLE
View Details →
EBC
1980-11-24
CONTACT SEAL
View Details →
JHJ
1980-11-24
ANSWER AT-HOME PREGNANCY TEST KIT
View Details →
DIF
1980-11-24
CARDIOACTIVE DRUGS CONTROL
View Details →
BYL
1980-11-24
MEDIUM SIZE OXYGEN HOOD #1547
View Details →
ITG
1980-11-24
CELLAMIN
View Details →
KLE
1980-11-24
HELIOBOND
View Details →
EAY
1980-11-24
HELIOMAT
View Details →No matching devices.
Page 13303 of 14146
Advertisement