6 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AIROS 8 Sequential Compression Device
FDA 510(k)
FDA Class 2
·Cardiovascular
CERALAS D 980NM DIODE LASER, MODELS D15 AND D25
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
EMIT II PLUS6-ACETYLMORPHINE ASSAY; EMIT II PLUS 6-AM/ ECSTASY CALIBRATOR/ CONTROL LEVEL 1; EMIT II PLUS 6-AM / ECTASY C
FDA 510(k)
FDA Class 2
·Clinical Toxicology
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·May 31, 2013
ACCESS® HTSH REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JLW·July 22, 2011
AISYS
FDA Adverse Event
Other
·DATEX-OHMEDA·Product code BSZ·September 18, 2008