WLP SEQUENTIAL VERSION MODEL WLP SOLO VI, WLP SOLO SEQUENTIAL

Sleeve, Limb, Compressible

WRIGHT LINEAR PUMP, INC.

The following data is part of a premarket notification filed by Wright Linear Pump, Inc. with the FDA for Wlp Sequential Version Model Wlp Solo Vi, Wlp Solo Sequential.

Pre-market Notification Details

Device IDK961292
510k NumberK961292
Device Name:WLP SEQUENTIAL VERSION MODEL WLP SOLO VI, WLP SOLO SEQUENTIAL
ClassificationSleeve, Limb, Compressible
Applicant WRIGHT LINEAR PUMP, INC. 408 NORTH TAYLOR AVE. Pittsburgh,  PA  15212
ContactJoe Soriero
CorrespondentJoe Soriero
WRIGHT LINEAR PUMP, INC. 408 NORTH TAYLOR AVE. Pittsburgh,  PA  15212
Product CodeJOW  
CFR Regulation Number870.5800 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1996-04-04
Decision Date1996-11-06
Summary:summary

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