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FDA 510(k)

ECG INTERFERENCE FILTER TF-03

K-Number: K832888 · 1984-01-18

Decision Date1984-01-18
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ECG INTERFERENCE FILTER TF-03 is the device name listed in this FDA 510(k) record. The listed applicant is La Jolla Technology, Inc.. It received FDA 510(k) clearance on 1984-01-18 under 510(k) number K832888. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECG INTERFERENCE FILTER TF-03?

ECG INTERFERENCE FILTER TF-03 is a medical device that received FDA 510(k) clearance on 1984-01-18. The listed applicant is La Jolla Technology, Inc.. The 510(k) number is K832888.

When did ECG INTERFERENCE FILTER TF-03 receive FDA 510(k) clearance?

ECG INTERFERENCE FILTER TF-03 received FDA 510(k) clearance on 1984-01-18, under 510(k) number K832888.

Who is the listed applicant for ECG INTERFERENCE FILTER TF-03?

The FDA 510(k) record lists La Jolla Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ECG INTERFERENCE FILTER TF-03?

The FDA product code for ECG INTERFERENCE FILTER TF-03 is DPS.

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 La Jolla Technology, Inc. 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.

Related Devices (Code: DPS)

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

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

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