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FDA 510(k)

ECG CABLES, TRUNK AND PATIENT LEAD WIRES

K-Number: K070232 · 2007-03-27

ApplicantAmerican I.V. Products, Inc.
Decision Date2007-03-27
Product CodeDSA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ECG CABLES, TRUNK AND PATIENT LEAD WIRES is the device name listed in this FDA 510(k) record. The listed applicant is American I.V. Products, Inc.. It received FDA 510(k) clearance on 2007-03-27 under 510(k) number K070232. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECG CABLES, TRUNK AND PATIENT LEAD WIRES?

ECG CABLES, TRUNK AND PATIENT LEAD WIRES is a medical device that received FDA 510(k) clearance on 2007-03-27. The listed applicant is American I.V. Products, Inc.. The 510(k) number is K070232.

When did ECG CABLES, TRUNK AND PATIENT LEAD WIRES receive FDA 510(k) clearance?

ECG CABLES, TRUNK AND PATIENT LEAD WIRES received FDA 510(k) clearance on 2007-03-27, under 510(k) number K070232.

Who is the listed applicant for ECG CABLES, TRUNK AND PATIENT LEAD WIRES?

The FDA 510(k) record lists American I.V. Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ECG CABLES, TRUNK AND PATIENT LEAD WIRES?

The FDA product code for ECG CABLES, TRUNK AND PATIENT LEAD WIRES is DSA.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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