FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
DCK
1979-12-31
DHR
1979-12-31
AGGLUTINOTEST-RHEUMATOID ARTHRITIS
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BZK
1979-12-31
ALARM USED W/MONITORING SPIROMETER
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JIX
1979-12-31
SERACON-SRI (PROD. # D029
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GYK
1979-12-31
H-H SHUNT INTRODUCER
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JTZ
1979-12-31
CULTURE PLATES & TUBED MEDIA
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GGP
1979-12-31
HELENA FACTOR IX DEFICIENT SUBSTRATE
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JIX
1979-12-31
SERACON-SRI
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JSE
1979-12-31
SIM MEDIUM
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JSH
1979-12-31
VOGEL-JOHNSON AGAR
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JZO
1979-12-31
AGGLUTINOTEST-THYROGLOBULIN
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DTB
1979-12-31
LIFELINE TLE ENDOCARDIAL PACING LEAD,
View Details →No matching devices.
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