L.E. DEMETRON II
K-Number: K051545 · 2005-07-18
Advertisement
Device Summary
Frequently Asked Questions
What is the L.E. DEMETRON II?
L.E. DEMETRON II is a medical device that received FDA 510(k) clearance on 2005-07-18. The listed applicant is Kerr Corporation (Danbury). The 510(k) number is K051545.
When did L.E. DEMETRON II receive FDA 510(k) clearance?
L.E. DEMETRON II received FDA 510(k) clearance on 2005-07-18, under 510(k) number K051545.
Who is the listed applicant for L.E. DEMETRON II?
The FDA 510(k) record lists Kerr Corporation (Danbury) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for L.E. DEMETRON II?
The FDA product code for L.E. DEMETRON II 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 Kerr Corporation (Danbury) 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.
Advertisement