QUANTEC SERIES 2000 ENDODONTIC FILES
K-Number: K962031 · 1996-06-04
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Device Summary
Frequently Asked Questions
What is the QUANTEC SERIES 2000 ENDODONTIC FILES?
QUANTEC SERIES 2000 ENDODONTIC FILES is a medical device that received FDA 510(k) clearance on 1996-06-04. The listed applicant is Tycom Dental. The 510(k) number is K962031.
When did QUANTEC SERIES 2000 ENDODONTIC FILES receive FDA 510(k) clearance?
QUANTEC SERIES 2000 ENDODONTIC FILES received FDA 510(k) clearance on 1996-06-04, under 510(k) number K962031.
Who is the listed applicant for QUANTEC SERIES 2000 ENDODONTIC FILES?
The FDA 510(k) record lists Tycom Dental as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QUANTEC SERIES 2000 ENDODONTIC FILES?
The FDA product code for QUANTEC SERIES 2000 ENDODONTIC FILES is EKS.
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 Tycom Dental 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: EKS)
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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