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FDA 510(k)

MENSOR COMPLIANT KEEPER

K-Number: K885158 · 1991-06-06

ApplicantMerrill C. Mensor, Jr., D.D.S.
Decision Date1991-06-06
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MENSOR COMPLIANT KEEPER 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 1991-06-06 under 510(k) number K885158. 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 COMPLIANT KEEPER?

MENSOR COMPLIANT KEEPER is a medical device that received FDA 510(k) clearance on 1991-06-06. The listed applicant is Merrill C. Mensor, Jr., D.D.S.. The 510(k) number is K885158.

When did MENSOR COMPLIANT KEEPER receive FDA 510(k) clearance?

MENSOR COMPLIANT KEEPER received FDA 510(k) clearance on 1991-06-06, under 510(k) number K885158.

Who is the listed applicant for MENSOR COMPLIANT KEEPER?

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 COMPLIANT KEEPER?

The FDA product code for MENSOR COMPLIANT KEEPER 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.

K885159MENSOR MAGNASKIRT

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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