DENTURE ADJUSTMENT KIT
K-Number: K820685 · 1982-04-09
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Device Summary
Frequently Asked Questions
What is the DENTURE ADJUSTMENT KIT?
DENTURE ADJUSTMENT KIT is a medical device that received FDA 510(k) clearance on 1982-04-09. The listed applicant is Camdent Laboratories. The 510(k) number is K820685.
When did DENTURE ADJUSTMENT KIT receive FDA 510(k) clearance?
DENTURE ADJUSTMENT KIT received FDA 510(k) clearance on 1982-04-09, under 510(k) number K820685.
Who is the listed applicant for DENTURE ADJUSTMENT KIT?
The FDA 510(k) record lists Camdent Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DENTURE ADJUSTMENT KIT?
The FDA product code for DENTURE ADJUSTMENT KIT is EBO.
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: EBO)
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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