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FDA 510(k)

ELECTRODE TESTER

K-Number: K780501 · 1978-05-19

ApplicantMg Medical Electronics
Decision Date1978-05-19
Product CodeKRC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTRODE TESTER is the device name listed in this FDA 510(k) record. The listed applicant is Mg Medical Electronics. It received FDA 510(k) clearance on 1978-05-19 under 510(k) number K780501. The device is classified under product code KRC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRODE TESTER?

ELECTRODE TESTER is a medical device that received FDA 510(k) clearance on 1978-05-19. The listed applicant is Mg Medical Electronics. The 510(k) number is K780501.

When did ELECTRODE TESTER receive FDA 510(k) clearance?

ELECTRODE TESTER received FDA 510(k) clearance on 1978-05-19, under 510(k) number K780501.

Who is the listed applicant for ELECTRODE TESTER?

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

What is the FDA product code for ELECTRODE TESTER?

The FDA product code for ELECTRODE TESTER is KRC.

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Related Devices (Code: KRC)

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.

K023713SONOPREP IMPEDANCE DIAGNOSTICS (IDX) SYSTEM, MODEL D1000Sontra Medical, Inc.K872370BIOMA 3500E.B.S., Inc.K874327SKIN PREP ANALYZERMarquette Electronics, Inc.K874155CIRCAMED MONITOR REMOTE START CONDUCTANCE METERCircadian, Inc.K840358IMPEDANCE/8200 MONITOR-MODEL 8300Aequitron Medical, Inc.K833619CONDUCTANCE METERCircadian, Inc.

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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