SURGERY BRUSH
K-Number: K782173 · 1979-01-10
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Device Summary
Frequently Asked Questions
What is the SURGERY BRUSH?
SURGERY BRUSH is a medical device that received FDA 510(k) clearance on 1979-01-10. The listed applicant is Dexide, Inc.. The 510(k) number is K782173.
When did SURGERY BRUSH receive FDA 510(k) clearance?
SURGERY BRUSH received FDA 510(k) clearance on 1979-01-10, under 510(k) number K782173.
Who is the listed applicant for SURGERY BRUSH?
The FDA 510(k) record lists Dexide, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SURGERY BRUSH?
The FDA product code for SURGERY BRUSH is GEC.
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 Dexide, 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: GEC)
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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