MINICAM
K-Number: K001541 · 2000-07-21
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Device Summary
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
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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