DEN-MAT FIBER OPTIC HALOGEN LIGHT
K-Number: K802716 · 1980-11-12
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Device Summary
Frequently Asked Questions
What is the DEN-MAT FIBER OPTIC HALOGEN LIGHT?
DEN-MAT FIBER OPTIC HALOGEN LIGHT is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Den-Mat Corp.. The 510(k) number is K802716.
When did DEN-MAT FIBER OPTIC HALOGEN LIGHT receive FDA 510(k) clearance?
DEN-MAT FIBER OPTIC HALOGEN LIGHT received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802716.
Who is the listed applicant for DEN-MAT FIBER OPTIC HALOGEN LIGHT?
The FDA 510(k) record lists Den-Mat Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEN-MAT FIBER OPTIC HALOGEN LIGHT?
The FDA product code for DEN-MAT FIBER OPTIC HALOGEN LIGHT is EAY.
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 Den-Mat Corp. 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: EAY)
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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