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FDA 510(k)

MEDA CROWN SERIES

K-Number: K913800 · 1991-10-04

ApplicantMedical Electronic Assn.
Decision Date1991-10-04
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDA CROWN SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Medical Electronic Assn.. It received FDA 510(k) clearance on 1991-10-04 under 510(k) number K913800. 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 MEDA CROWN SERIES?

MEDA CROWN SERIES is a medical device that received FDA 510(k) clearance on 1991-10-04. The listed applicant is Medical Electronic Assn.. The 510(k) number is K913800.

When did MEDA CROWN SERIES receive FDA 510(k) clearance?

MEDA CROWN SERIES received FDA 510(k) clearance on 1991-10-04, under 510(k) number K913800.

Who is the listed applicant for MEDA CROWN SERIES?

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

What is the FDA product code for MEDA CROWN SERIES?

The FDA product code for MEDA CROWN SERIES is GZJ.

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Other records listing Medical Electronic Assn. 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.

K882943MEDA ONE-STEPK862011MULTI-DAY ELECTRODES

Related Devices (Code: GZJ)

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

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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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