DENTAL LIGHT
K-Number: K926081 · 1994-01-26
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Device Summary
Frequently Asked Questions
What is the DENTAL LIGHT?
DENTAL LIGHT is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Mdt Corp., Inc.. The 510(k) number is K926081.
When did DENTAL LIGHT receive FDA 510(k) clearance?
DENTAL LIGHT received FDA 510(k) clearance on 1994-01-26, under 510(k) number K926081.
Who is the listed applicant for DENTAL LIGHT?
The FDA 510(k) record lists Mdt Corp., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DENTAL LIGHT?
The FDA product code for DENTAL LIGHT is EAZ.
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 Mdt Corp., 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: EAZ)
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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