COX DISPOSABLE CYTOLOGY BRUSHES
K-Number: K912407 · 1991-09-10
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Device Summary
Frequently Asked Questions
What is the COX DISPOSABLE CYTOLOGY BRUSHES?
COX DISPOSABLE CYTOLOGY BRUSHES is a medical device that received FDA 510(k) clearance on 1991-09-10. The listed applicant is Cox Medical Ent., Inc.. The 510(k) number is K912407.
When did COX DISPOSABLE CYTOLOGY BRUSHES receive FDA 510(k) clearance?
COX DISPOSABLE CYTOLOGY BRUSHES received FDA 510(k) clearance on 1991-09-10, under 510(k) number K912407.
Who is the listed applicant for COX DISPOSABLE CYTOLOGY BRUSHES?
The FDA 510(k) record lists Cox Medical Ent., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COX DISPOSABLE CYTOLOGY BRUSHES?
The FDA product code for COX DISPOSABLE CYTOLOGY BRUSHES is FDX.
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 Cox Medical Ent., 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: FDX)
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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