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FDA 510(k)

MINICAM

K-Number: K001541 · 2000-07-21

Decision Date2000-07-21
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MINICAM is the device name listed in this FDA 510(k) record. The listed applicant is Video Dental Concepts, Inc.. It received FDA 510(k) clearance on 2000-07-21 under 510(k) number K001541. 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 MINICAM?

MINICAM is a medical device that received FDA 510(k) clearance on 2000-07-21. The listed applicant is Video Dental Concepts, Inc.. The 510(k) number is K001541.

When did MINICAM receive FDA 510(k) clearance?

MINICAM received FDA 510(k) clearance on 2000-07-21, under 510(k) number K001541.

Who is the listed applicant for MINICAM?

The FDA 510(k) record lists Video Dental Concepts, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINICAM?

The FDA product code for MINICAM 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 Video Dental Concepts, Inc. 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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