CLEARVIEW DENTAL HANDPIECE LUBRICATOR AND LUBRICANT
K-Number: K070297 · 2007-02-05
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Device Summary
Frequently Asked Questions
What is the CLEARVIEW DENTAL HANDPIECE LUBRICATOR AND LUBRICANT?
CLEARVIEW DENTAL HANDPIECE LUBRICATOR AND LUBRICANT is a medical device that received FDA 510(k) clearance on 2007-02-05. The listed applicant is Dental Air Solutions of Nc, Inc.. The 510(k) number is K070297.
When did CLEARVIEW DENTAL HANDPIECE LUBRICATOR AND LUBRICANT receive FDA 510(k) clearance?
CLEARVIEW DENTAL HANDPIECE LUBRICATOR AND LUBRICANT received FDA 510(k) clearance on 2007-02-05, under 510(k) number K070297.
Who is the listed applicant for CLEARVIEW DENTAL HANDPIECE LUBRICATOR AND LUBRICANT?
The FDA 510(k) record lists Dental Air Solutions of Nc, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLEARVIEW DENTAL HANDPIECE LUBRICATOR AND LUBRICANT?
The FDA product code for CLEARVIEW DENTAL HANDPIECE LUBRICATOR AND LUBRICANT is EFB.
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.
Related Devices (Code: EFB)
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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