Vectraplexecg System with Vectraplexami

FDA 510(k) K102378 · Vectracor, Inc.

Substantially Equivalent

510(k) numberK102378

Submission

Device name
Vectraplexecg System with Vectraplexami
Applicant
Vectracor, Inc.
Totowa, NJ, US
Received
August 20, 2010
Decision date
November 2, 2011
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DPS – Electrocardiograph
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2340
Specialty
Cardiovascular

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K243305Masimo W1DPS · Traditional Masimo Corporation04/03/2025SE
K241217CloudHRV™ System (100-01-001)DPS · Traditional Inmedix, Inc.01/16/2025SE
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K240229Masimo W1DPS · Traditional Masimo Corporation08/08/2024SE

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Questions and answers

When was Vectraplexecg System with Vectraplexami cleared by the FDA?

Vectraplexecg System with Vectraplexami (K102378) received a 510(k) decision of Substantially Equivalent on November 2, 2011, 439 days after the submission was received.

What is the product code of K102378?

The FDA product code is DPS – Electrocardiograph, a Class II (moderate risk) device regulated under 21 CFR 870.2340.