CERAMIST BRUSH
K-Number: K770160 · 1977-01-31
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Device Summary
Frequently Asked Questions
What is the CERAMIST BRUSH?
CERAMIST BRUSH is a medical device that received FDA 510(k) clearance on 1977-01-31. The listed applicant is Deringer-Ney, Inc.. The 510(k) number is K770160.
When did CERAMIST BRUSH receive FDA 510(k) clearance?
CERAMIST BRUSH received FDA 510(k) clearance on 1977-01-31, under 510(k) number K770160.
Who is the listed applicant for CERAMIST BRUSH?
The FDA 510(k) record lists Deringer-Ney, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CERAMIST BRUSH?
The FDA product code for CERAMIST BRUSH is KXR.
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 Deringer-Ney, 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: KXR)
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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