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FDA 510(k)

DISPOSABLE ECG MONITORING ELECTRODES, MODELS, 4420, 4440

K-Number: K990115 · 1999-12-06

Decision Date1999-12-06
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE ECG MONITORING ELECTRODES, MODELS, 4420, 4440 is the device name listed in this FDA 510(k) record. The listed applicant is Maersk Medical A/S. It received FDA 510(k) clearance on 1999-12-06 under 510(k) number K990115. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE ECG MONITORING ELECTRODES, MODELS, 4420, 4440?

DISPOSABLE ECG MONITORING ELECTRODES, MODELS, 4420, 4440 is a medical device that received FDA 510(k) clearance on 1999-12-06. The listed applicant is Maersk Medical A/S. The 510(k) number is K990115.

When did DISPOSABLE ECG MONITORING ELECTRODES, MODELS, 4420, 4440 receive FDA 510(k) clearance?

DISPOSABLE ECG MONITORING ELECTRODES, MODELS, 4420, 4440 received FDA 510(k) clearance on 1999-12-06, under 510(k) number K990115.

Who is the listed applicant for DISPOSABLE ECG MONITORING ELECTRODES, MODELS, 4420, 4440?

The FDA 510(k) record lists Maersk Medical A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE ECG MONITORING ELECTRODES, MODELS, 4420, 4440?

The FDA product code for DISPOSABLE ECG MONITORING ELECTRODES, MODELS, 4420, 4440 is DRX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Maersk Medical A/S as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 9 devices →

Related Devices (Code: DRX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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