BEECH VERSA LOK

Set, Administration, Intravascular

BEECH MEDICAL PRODUCTS, INC.

The following data is part of a premarket notification filed by Beech Medical Products, Inc. with the FDA for Beech Versa Lok.

Pre-market Notification Details

Device IDK933749
510k NumberK933749
Device Name:BEECH VERSA LOK
ClassificationSet, Administration, Intravascular
Applicant BEECH MEDICAL PRODUCTS, INC. 16 SOUTH STATE ST. Newtown,  PA  18940
ContactJohn Romano
CorrespondentJohn Romano
BEECH MEDICAL PRODUCTS, INC. 16 SOUTH STATE ST. Newtown,  PA  18940
Product CodeFPA  
CFR Regulation Number880.5440 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1993-08-03
Decision Date1993-12-29

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