NORFOLK NORPORT, SUBCUT. IMPLANTED DRUG DEL. 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, Subcut. Implanted Drug Del. Depot.

Pre-market Notification Details

Device IDK870187
510k NumberK870187
Device Name:NORFOLK NORPORT, SUBCUT. IMPLANTED DRUG DEL. 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 Received1987-01-16
Decision Date1987-05-07

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