DENTAL BURS
K-Number: K882183 · 1988-06-21
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Device Summary
Frequently Asked Questions
What is the DENTAL BURS?
DENTAL BURS is a medical device that received FDA 510(k) clearance on 1988-06-21. The listed applicant is Tri-Stage, Inc.. The 510(k) number is K882183.
When did DENTAL BURS receive FDA 510(k) clearance?
DENTAL BURS received FDA 510(k) clearance on 1988-06-21, under 510(k) number K882183.
Who is the listed applicant for DENTAL BURS?
The FDA 510(k) record lists Tri-Stage, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DENTAL BURS?
The FDA product code for DENTAL BURS is EJL.
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 Tri-Stage, 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: EJL)
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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