TEAM CARIES INDICATOR
K-Number: K963927 · 1996-11-15
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Device Summary
Frequently Asked Questions
What is the TEAM CARIES INDICATOR?
TEAM CARIES INDICATOR is a medical device that received FDA 510(k) clearance on 1996-11-15. The listed applicant is Centrix, Inc.. The 510(k) number is K963927.
When did TEAM CARIES INDICATOR receive FDA 510(k) clearance?
TEAM CARIES INDICATOR received FDA 510(k) clearance on 1996-11-15, under 510(k) number K963927.
Who is the listed applicant for TEAM CARIES INDICATOR?
The FDA 510(k) record lists Centrix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TEAM CARIES INDICATOR?
The FDA product code for TEAM CARIES INDICATOR is LFC.
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 Centrix, 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: LFC)
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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