NORFOLK NORPORT/SUBCUTAN. IMPLANTED DRUG DEPOT

Port & Catheter, Implanted, Subcutaneous, Intravascular

NORFOLK MEDICAL PRODUCTS, INC.

The following data is part of a premarket notification filed by Norfolk Medical Products, Inc. with the FDA for Norfolk Norport/subcutan. Implanted Drug Depot.

Pre-market Notification Details

Device IDK863723
510k NumberK863723
Device Name:NORFOLK NORPORT/SUBCUTAN. IMPLANTED DRUG DEPOT
ClassificationPort & Catheter, Implanted, Subcutaneous, Intravascular
Applicant NORFOLK MEDICAL PRODUCTS, INC. 7307 N. RIDGEWAY Skokie,  IL  60076
ContactMichael J Dalton
CorrespondentMichael J Dalton
NORFOLK MEDICAL PRODUCTS, INC. 7307 N. RIDGEWAY Skokie,  IL  60076
Product CodeLJT  
CFR Regulation Number880.5965 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1986-09-23
Decision Date1986-10-29

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.