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EP-Connect

FDA UDI

Class II (US FDA UDI)

by Cardio Command

Identity

Trade Name
EP-Connect FDA UDI
Generic Name
Electrocardiographic lead/catheter adaptor FDA UDI
Device Name
A 10 ft. cable that connects Model 1600 Octapolar catheter products to ECG recorders using modular to pin connector. FDA UDI
Model / Reference
Octapolar FDA UDI
Description
A 10 ft. cable that connects Model 1600 Octapolar catheter products to ECG recorders using modular to pin connector. FDA UDI

Identifiers

Catalog Number
8032 FDA UDI
Primary DI / UDI-DI
00856233005097 FDA UDI
510(k) Number
K905831 FDA UDI
FDA Product Code
DRF FDA UDI
GMDN Term
Electrocardiographic lead/catheter adaptor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1220 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrocardiographic lead/catheter adaptor

EP-Connect by Cardio Command — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic lead/catheter adaptor.

Cleared under the same submission

K905831 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardio Command

Sources (1)

  • FDA UDI 73695c21-fc98-4115-b67a-545748254066 36 fields · synced Jun 1, 2026