PALODENT MATRICES & BITINE RINGS
K-Number: K801142 · 1980-08-07
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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