L.E.DEMETRON
K-Number: K021797 · 2002-06-27
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Device Summary
Frequently Asked Questions
What is the L.E.DEMETRON?
L.E.DEMETRON is a medical device that received FDA 510(k) clearance on 2002-06-27. The listed applicant is Sybron Dental Specialties, Inc.. The 510(k) number is K021797.
When did L.E.DEMETRON receive FDA 510(k) clearance?
L.E.DEMETRON received FDA 510(k) clearance on 2002-06-27, under 510(k) number K021797.
Who is the listed applicant for L.E.DEMETRON?
The FDA 510(k) record lists Sybron Dental Specialties, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for L.E.DEMETRON?
The FDA product code for L.E.DEMETRON is EBZ.
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 Sybron Dental Specialties, 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: EBZ)
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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