FDA.reportPublic FDA data

EP Connect

Primary DI
00856233005080
Brand
EP Connect
Company
CARDIOCOMMAND, INC.
Model
Tapcath
Catalog number
8031-0001
Device description
A 10 ft. cable that connects Tapcath catheter products to ECG recorders using a modular to pin connector. .
Published
2015-04-03
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
DRFCatheter, Electrode Recording, Or Probe, Electrode Recording

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DRFCatheter, Electrode Recording, Or Probe, Electrode RecordingCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
P860008017
P860008019
P860008020

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
P860008017ARZCO TRANSESOPHAGEAL CARDIAC STIMULATOR MODEL 7Cardio Command1986-12-30LPA
P860008019ARZCO TRANSESOPHAGEAL CARDIAC STIMULATOR MODEL 7Cardio Command1986-12-30LPA
P860008020ARZCO TRANSESOPHAGEAL CARDIAC STIMULATOR MODEL 7Cardio Command1986-12-30LPA

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00856233005080PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00856233005080008562330050808562330050800856233005080

GMDN Terms#

Term, Definition table
TermDefinition
Electrocardiographic lead/catheter adaptorA small, sterile, connecting device that enables a mechanical union between an in situ cardiac catheter [e.g., an electrophysiology (EP) diagnostic catheter] and an electrocardiograph (ECG) cable/lead for transmission of heart signals to an ECG machine. This device allows the connection of the otherwise incompatible connectors of the cardiac catheter to a standard ECG cable/lead or a cable/lead of different manufacture. This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
(800) 231-6370cconley@CardiCommand.com

Regulatory Flags#

DUNS number
800214827
Device count
1
Lot or batch
true
Manufacturing date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00856233005127Model 7ALeft arm patient lead wire80212015-04-03
00856233005134Model 7ARight arm patient lead wire80232015-04-03
10856233005063Tapsystem2A, single pack8002A2015-07-22
10856233005155Tapsystem2A re-man'd, single pack8002A-99992015-07-22
10856233005162Model 7ASingle pack01012015-04-03
10856233005179Model 7ARe-manufactured, single pack0101-99992015-04-03
00856233005066Tapsystem2A, unpackaged8002A2015-07-22
00856233005110Model 7A7A/Mod 3 Interface cable04062015-04-03
00856233005158Tapsystem2A re-man'd, unpackaged8002A-99992015-07-22
00856233005165Model 7AUnpackaged01012015-04-03
00856233005172Model 7ARe-manufactured, unpackaged0101-99992015-04-03
10856233005186Model 3Single pack01042015-04-03
10856233005193Model 3Re-manufactured, single pack0104-99992015-04-03
00856233005004Tapscope550, single pack2002015-04-03
00856233005011Tapscope550F, single pack2502015-04-08
00856233005028Tapscope210, single pack1002015-04-03
00856233005035Tapscope210-S, single pack1022015-04-03
00856233005042Tapcath205, single pack1802015-04-03
00856233005059Tapcath1600, single pack16002015-07-22
00856233005073Tapsystem2A Patient Cable20102015-07-22

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Primary DI, Brand, Company table
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00818087023054MAGiC SweepACCESS POINT TECHNOLOGIES, INC.DRF2026-05-15
00818087023061MAGiC SweepACCESS POINT TECHNOLOGIES, INC.DRF2026-05-15
00818087023085MAGiC SweepACCESS POINT TECHNOLOGIES, INC.DRF2026-05-15
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