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FDA 510(k)

THE MEHESZ STIMULATING SYSTEM

K-Number: K844994 · 1985-03-06

ApplicantCampden Medical , Ltd.
Decision Date1985-03-06
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

THE MEHESZ STIMULATING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Campden Medical , Ltd.. It received FDA 510(k) clearance on 1985-03-06 under 510(k) number K844994. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE MEHESZ STIMULATING SYSTEM?

THE MEHESZ STIMULATING SYSTEM is a medical device that received FDA 510(k) clearance on 1985-03-06. The listed applicant is Campden Medical , Ltd.. The 510(k) number is K844994.

When did THE MEHESZ STIMULATING SYSTEM receive FDA 510(k) clearance?

THE MEHESZ STIMULATING SYSTEM received FDA 510(k) clearance on 1985-03-06, under 510(k) number K844994.

Who is the listed applicant for THE MEHESZ STIMULATING SYSTEM?

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

What is the FDA product code for THE MEHESZ STIMULATING SYSTEM?

The FDA product code for THE MEHESZ STIMULATING SYSTEM is GZJ.

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Related Devices (Code: GZJ)

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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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