ACUITY™ Steerable

GUDID 00802526419447

Coronary Venous Steroid-Eluting Bipolar Pace/Sense Lead

BOSTON SCIENTIFIC CORPORATION

Endocardial pacing lead Endocardial pacing lead Endocardial pacing lead Endocardial pacing lead Endocardial pacing lead Endocardial pacing lead Endocardial pacing lead Endocardial pacing lead Endocardial pacing lead Endocardial pacing lead Endocardial pacing lead Endocardial pacing lead Endocardial pacing lead Endocardial/interventricular septal pacing lead Endocardial/interventricular septal pacing lead Endocardial/interventricular septal pacing lead Endocardial/interventricular septal pacing lead Endocardial/interventricular septal pacing lead Endocardial/interventricular septal pacing lead Endocardial/interventricular septal pacing lead Endocardial/interventricular septal pacing lead Endocardial/interventricular septal pacing lead Endocardial/interventricular septal pacing lead Endocardial/interventricular septal pacing lead Endocardial/interventricular septal pacing lead Endocardial/interventricular septal pacing lead Endocardial/interventricular septal pacing lead Endocardial/interventricular septal pacing lead Endocardial/interventricular septal pacing lead Endocardial/interventricular septal pacing lead
Primary Device ID00802526419447
NIH Device Record Key44bba984-5b0e-4763-b71b-84b6f86c7165
Commercial Distribution StatusIn Commercial Distribution
Brand NameACUITY™ Steerable
Version Model Number4555
Company DUNS106295384
Company NameBOSTON SCIENTIFIC CORPORATION
Device Count1
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Producttrue
Single Usetrue
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

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Device Identifiers

Device Issuing AgencyDevice ID
GS100802526419447 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NVYPermanent defibrillator electrodes

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2014-09-24

On-Brand Devices [ACUITY™ Steerable]

00802526419447Coronary Venous Steroid-Eluting Bipolar Pace/Sense Lead
00802526419324Coronary Venous Steroid-Eluting Bipolar Pace/Sense Lead

Trademark Results [ACUITY]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ACUITY
ACUITY
98265405 not registered Live/Pending
CAO Group, Inc.
2023-11-10
ACUITY
ACUITY
98109018 not registered Live/Pending
DSD Partners, LLC
2023-07-31
ACUITY
ACUITY
97895530 not registered Live/Pending
Kaplan Moreno, Skylar
2023-04-19
ACUITY
ACUITY
97749331 not registered Live/Pending
Aderis Energy, LLC
2023-01-11
ACUITY
ACUITY
97529110 not registered Live/Pending
Applied Materials, Inc.
2022-08-01
ACUITY
ACUITY
90177063 not registered Live/Pending
RYTY PARTNERS LLC
2020-09-13
ACUITY
ACUITY
90109701 not registered Live/Pending
BreviTest Technologies, LLC
2020-08-12
ACUITY
ACUITY
90092798 not registered Live/Pending
Acist Medical Systems, Inc.
2020-08-04
ACUITY
ACUITY
88887664 not registered Live/Pending
Acuity Ag Solutions, LLC
2020-04-25
ACUITY
ACUITY
88876157 not registered Live/Pending
MEDIVIEW XR, INC.
2020-04-17
ACUITY
ACUITY
88460503 not registered Live/Pending
Johnson, Grossnickle and Associates, Inc.
2019-06-05
ACUITY
ACUITY
88433321 5931050 Live/Registered
California Clinic Management
2019-05-16

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