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FDA 510(k)

RICH-MAR CARBON ELECTRODES

K-Number: K950491 · 1995-03-29

Decision Date1995-03-29
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

RICH-MAR CARBON ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Rich-Mar Corp.. It received FDA 510(k) clearance on 1995-03-29 under 510(k) number K950491. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RICH-MAR CARBON ELECTRODES?

RICH-MAR CARBON ELECTRODES is a medical device that received FDA 510(k) clearance on 1995-03-29. The listed applicant is Rich-Mar Corp.. The 510(k) number is K950491.

When did RICH-MAR CARBON ELECTRODES receive FDA 510(k) clearance?

RICH-MAR CARBON ELECTRODES received FDA 510(k) clearance on 1995-03-29, under 510(k) number K950491.

Who is the listed applicant for RICH-MAR CARBON ELECTRODES?

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

What is the FDA product code for RICH-MAR CARBON ELECTRODES?

The FDA product code for RICH-MAR CARBON ELECTRODES is GXY.

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 Rich-Mar Corp. 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 43 devices →

Related Devices (Code: GXY)

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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