BLUWHITE DIAMOND DENTAL BURS MODIFIED
K-Number: K120037 · 2012-04-20
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Device Summary
Frequently Asked Questions
What is the BLUWHITE DIAMOND DENTAL BURS MODIFIED?
BLUWHITE DIAMOND DENTAL BURS MODIFIED is a medical device that received FDA 510(k) clearance on 2012-04-20. The listed applicant is Beavers Dental, Div. Sybron Canada, Ltd.. The 510(k) number is K120037.
When did BLUWHITE DIAMOND DENTAL BURS MODIFIED receive FDA 510(k) clearance?
BLUWHITE DIAMOND DENTAL BURS MODIFIED received FDA 510(k) clearance on 2012-04-20, under 510(k) number K120037.
Who is the listed applicant for BLUWHITE DIAMOND DENTAL BURS MODIFIED?
The FDA 510(k) record lists Beavers Dental, Div. Sybron Canada, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLUWHITE DIAMOND DENTAL BURS MODIFIED?
The FDA product code for BLUWHITE DIAMOND DENTAL BURS MODIFIED is DZP.
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 Beavers Dental, Div. Sybron Canada, Ltd. 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: DZP)
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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