ULTRACAM
K-Number: K933671 · 1994-03-31
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Device Summary
Frequently Asked Questions
What is the ULTRACAM?
ULTRACAM is a medical device that received FDA 510(k) clearance on 1994-03-31. The listed applicant is Dental Vision Direct, Inc.. The 510(k) number is K933671.
When did ULTRACAM receive FDA 510(k) clearance?
ULTRACAM received FDA 510(k) clearance on 1994-03-31, under 510(k) number K933671.
Who is the listed applicant for ULTRACAM?
The FDA 510(k) record lists Dental Vision Direct, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ULTRACAM?
The FDA product code for ULTRACAM 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 Dental Vision Direct, 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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