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FDA 510(k)

INTRAORAL CAMERA ME-15

K-Number: K020206 · 2002-04-11

Decision Date2002-04-11
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTRAORAL CAMERA ME-15 is the device name listed in this FDA 510(k) record. The listed applicant is Dent Corp. Research & Development. It received FDA 510(k) clearance on 2002-04-11 under 510(k) number K020206. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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

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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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