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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 PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DevicePORT-A-CATH EPIDURAL/PORT-A-CATH II LOW PROFILE EPIDURAL SYSTEMS
Generic NameCATHETER, PERCUTANEOUS, LONG TERM, INTRASPINAL
ApplicantSmiths Medical Asd, Inc.
1265 Grey Fox Rd.
St. Paul, MN 55112
PMA NumberP900052
Supplement NumberS011
Date Received09/04/2002
Decision Date10/03/2002
Withdrawal Date12/26/2018
Product Code LNY 
Advisory Committee General Hospital
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
CHANGE IN THE METHOD OF MARKING THE PRODUCT NAME AND LOT NUMBER ON THE PORTAL RESERVOIRS FROM ENGRAVING TO LASER MARKING.
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