FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
KIJ
1982-10-22
IKZ
1982-10-22
ROTO REST KINETIC TREATMENT TABLE PEDIA
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EIL
1982-10-22
PIO ROOT CANAL INDICATOR
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CAW
1982-10-22
MODEL #6200 OXYGEN CONCENTRATOR
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EJS
1982-10-22
RX UNIVERSAL
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BXK
1982-10-22
CLINICAL GAS MIXTURE-NON-FLAMMABLE
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EQH
1982-10-22
LARYNGEAL SPATULAS
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FDF
1982-10-22
PENTAX FC-38LA & FC-38SA COLONOFIBER
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CAW
1982-10-22
MODEL BX-3000 OXYGEN CONCENTRATOR
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DGC
1982-10-22
RAST ALLERCOAT ALLERGEN DISCS
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EJH
1982-10-22
CAVIDRY
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N/A
1982-10-22
OPERAND SUTURE REMOVAL TRAY
View Details →No matching devices.
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