FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
DRM
1980-02-05
GYB
1980-02-05
ECA GEL
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IYO
1980-02-05
UCA GEL
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BTL
1980-02-05
PNEUPAC OXYGEN THERAPY UNIT
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DXY
1980-02-05
PULSE GENERATOR, MODEL NO. LIT 222
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CGA
1980-02-05
GLUCOSE OXIDASE REAGENT KIT
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GEX
1980-02-05
SHARPLAN 743, CO2 LASER SURGICAL SYSTEM
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IPF
1980-02-05
ELECTRICAL MUSCLE STIMULATOR (EMS)
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IYO
1980-02-05
UCA CREAM
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LCD
1980-02-05
EMIT TOBRAMYCIN ASSAY
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DRM
1980-02-05
PNEUPAC TEST SET, PT.#500-A250
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DRM
1980-02-05
PNEUPAC RESUSCITATOR INSTANT ACTION SET
View Details →No matching devices.
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