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FDA 510(k)

MENSOR MAGNASKIRT

K-Number: K885159 · 1990-04-19

ApplicantMerrill C. Mensor, Jr., D.D.S.
Decision Date1990-04-19
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MENSOR MAGNASKIRT is the device name listed in this FDA 510(k) record. The listed applicant is Merrill C. Mensor, Jr., D.D.S.. It received FDA 510(k) clearance on 1990-04-19 under 510(k) number K885159. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENSOR MAGNASKIRT?

MENSOR MAGNASKIRT is a medical device that received FDA 510(k) clearance on 1990-04-19. The listed applicant is Merrill C. Mensor, Jr., D.D.S.. The 510(k) number is K885159.

When did MENSOR MAGNASKIRT receive FDA 510(k) clearance?

MENSOR MAGNASKIRT received FDA 510(k) clearance on 1990-04-19, under 510(k) number K885159.

Who is the listed applicant for MENSOR MAGNASKIRT?

The FDA 510(k) record lists Merrill C. Mensor, Jr., D.D.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MENSOR MAGNASKIRT?

The FDA product code for MENSOR MAGNASKIRT is DZE.

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.

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Other records listing Merrill C. Mensor, Jr., D.D.S. 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.

K885158MENSOR COMPLIANT KEEPER

Related Devices (Code: DZE)

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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