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FDA 510(k)

PALODENT MATRICES & BITINE RINGS

K-Number: K801142 · 1980-08-07

Decision Date1980-08-07
Product CodeDZN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PALODENT MATRICES & BITINE RINGS is the device name listed in this FDA 510(k) record. The listed applicant is Alvin Meyer, D.D.S.. It received FDA 510(k) clearance on 1980-08-07 under 510(k) number K801142. The device is classified under product code DZN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PALODENT MATRICES & BITINE RINGS?

PALODENT MATRICES & BITINE RINGS is a medical device that received FDA 510(k) clearance on 1980-08-07. The listed applicant is Alvin Meyer, D.D.S.. The 510(k) number is K801142.

When did PALODENT MATRICES & BITINE RINGS receive FDA 510(k) clearance?

PALODENT MATRICES & BITINE RINGS received FDA 510(k) clearance on 1980-08-07, under 510(k) number K801142.

Who is the listed applicant for PALODENT MATRICES & BITINE RINGS?

The FDA 510(k) record lists Alvin Meyer, D.D.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PALODENT MATRICES & BITINE RINGS?

The FDA product code for PALODENT MATRICES & BITINE RINGS is DZN.

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.

Related Devices (Code: DZN)

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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