INTRAORAL CAMERA ME-15
K-Number: K020206 · 2002-04-11
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Device Summary
Frequently Asked Questions
What is the INTRAORAL CAMERA ME-15?
INTRAORAL CAMERA ME-15 is a medical device that received FDA 510(k) clearance on 2002-04-11. The listed applicant is Dent Corp. Research & Development. The 510(k) number is K020206.
When did INTRAORAL CAMERA ME-15 receive FDA 510(k) clearance?
INTRAORAL CAMERA ME-15 received FDA 510(k) clearance on 2002-04-11, under 510(k) number K020206.
Who is the listed applicant for INTRAORAL CAMERA ME-15?
The FDA 510(k) record lists Dent Corp. Research & Development as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTRAORAL CAMERA ME-15?
The FDA product code for INTRAORAL CAMERA ME-15 is EIA.
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.
Other records listing Dent Corp. Research & Development 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.
Related Devices (Code: EIA)
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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