FDA 510(k)

PATIENT CABLES FOR MONITORING, I.E., ECG, EKG, SPO2, AND BP INTERFACE CABLES AND LEADWIRES

K-Number: K992524 · 2000-03-01

ApplicantAdvantage Medical Electronics, Inc.

Decision Date2000-03-01

Product CodeDSA

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

PATIENT CABLES FOR MONITORING, I.E., ECG, EKG, SPO2, AND BP INTERFACE CABLES AND LEADWIRES is the device name listed in this FDA 510(k) record. The listed applicant is Advantage Medical Electronics, Inc.. It received FDA 510(k) clearance on 2000-03-01 under 510(k) number K992524. 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 PATIENT CABLES FOR MONITORING, I.E., ECG, EKG, SPO2, AND BP INTERFACE CABLES AND LEADWIRES?

PATIENT CABLES FOR MONITORING, I.E., ECG, EKG, SPO2, AND BP INTERFACE CABLES AND LEADWIRES is a medical device that received FDA 510(k) clearance on 2000-03-01. The listed applicant is Advantage Medical Electronics, Inc.. The 510(k) number is K992524.

When did PATIENT CABLES FOR MONITORING, I.E., ECG, EKG, SPO2, AND BP INTERFACE CABLES AND LEADWIRES receive FDA 510(k) clearance?

PATIENT CABLES FOR MONITORING, I.E., ECG, EKG, SPO2, AND BP INTERFACE CABLES AND LEADWIRES received FDA 510(k) clearance on 2000-03-01, under 510(k) number K992524.

Who is the listed applicant for PATIENT CABLES FOR MONITORING, I.E., ECG, EKG, SPO2, AND BP INTERFACE CABLES AND LEADWIRES?

The FDA 510(k) record lists Advantage Medical Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT CABLES FOR MONITORING, I.E., ECG, EKG, SPO2, AND BP INTERFACE CABLES AND LEADWIRES?

The FDA product code for PATIENT CABLES FOR MONITORING, I.E., ECG, EKG, SPO2, AND BP INTERFACE CABLES AND LEADWIRES is DSA.

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Official Source

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