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FDA 510(k)

ELECTRODES, FERRIS ECG, TYPES 905,906

K-Number: K790305 · 1979-04-03

ApplicantFerris Mfg. Corp.
Decision Date1979-04-03
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTRODES, FERRIS ECG, TYPES 905,906 is the device name listed in this FDA 510(k) record. The listed applicant is Ferris Mfg. Corp.. It received FDA 510(k) clearance on 1979-04-03 under 510(k) number K790305. 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 ELECTRODES, FERRIS ECG, TYPES 905,906?

ELECTRODES, FERRIS ECG, TYPES 905,906 is a medical device that received FDA 510(k) clearance on 1979-04-03. The listed applicant is Ferris Mfg. Corp.. The 510(k) number is K790305.

When did ELECTRODES, FERRIS ECG, TYPES 905,906 receive FDA 510(k) clearance?

ELECTRODES, FERRIS ECG, TYPES 905,906 received FDA 510(k) clearance on 1979-04-03, under 510(k) number K790305.

Who is the listed applicant for ELECTRODES, FERRIS ECG, TYPES 905,906?

The FDA 510(k) record lists Ferris Mfg. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRODES, FERRIS ECG, TYPES 905,906?

The FDA product code for ELECTRODES, FERRIS ECG, TYPES 905,906 is DRX.

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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.

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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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