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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameCELLSIUS INTERFACE CABLES (AUTOCLAVABLE)
Classification Namecatheter, electrode recording, or probe, electrode recording
Generic Nameinterface or accessory cables
Regulation Number870.1220
ApplicantCORDIS WEBSTER, INC.
PMA NumberP950005
Supplement NumberS006
Date Received08/02/1999
Decision Date02/01/2000
Product Code
DRF[ Registered Establishments with DRF ]
Advisory Committee Cardiovascular
Expedited Review Granted? No
Combination Product No
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