MCPARLAND SCALP VEIN CATHETER

Catheter, Subclavian

RENAL SYSTEMS, INC.

The following data is part of a premarket notification filed by Renal Systems, Inc. with the FDA for Mcparland Scalp Vein Catheter.

Pre-market Notification Details

Device IDK821001
510k NumberK821001
Device Name:MCPARLAND SCALP VEIN CATHETER
ClassificationCatheter, Subclavian
Applicant RENAL SYSTEMS, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeLFJ  
CFR Regulation Number876.5540 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1982-04-08
Decision Date1982-07-22

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