Liverty™ TIPS Access Set

Introducer, Catheter

Bard Peripheral Vascular, Inc

The following data is part of a premarket notification filed by Bard Peripheral Vascular, Inc with the FDA for Liverty™ Tips Access Set.

Pre-market Notification Details

Device IDK221440
510k NumberK221440
Device Name:Liverty™ TIPS Access Set
ClassificationIntroducer, Catheter
Applicant Bard Peripheral Vascular, Inc 1625 West 3rd Street Tempe,  AZ  85281
ContactScott Johnson
CorrespondentPrithul Bom
REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul,  MN  55114
Product CodeDYB  
CFR Regulation Number870.1340 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedYes
Combination ProductNo
Date Received2022-05-17
Decision Date2022-05-31

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00382903064663 K221440 000

Trademark Results [Liverty]

Mark Image

Registration | Serial
Company
Trademark
Application Date
LIVERTY
LIVERTY
90469326 not registered Live/Pending
C. R. BARD, INC.
2021-01-15
LIVERTY
LIVERTY
85780089 4511776 Live/Registered
GOLDEN BIOTECHNOLOGY CORPORATION
2012-11-15

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