CYTOLOGY BRUSH
K-Number: K933628 · 1994-03-11
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Device Summary
Frequently Asked Questions
What is the CYTOLOGY BRUSH?
CYTOLOGY BRUSH is a medical device that received FDA 510(k) clearance on 1994-03-11. The listed applicant is Bioteque America, Inc.. The 510(k) number is K933628.
When did CYTOLOGY BRUSH receive FDA 510(k) clearance?
CYTOLOGY BRUSH received FDA 510(k) clearance on 1994-03-11, under 510(k) number K933628.
Who is the listed applicant for CYTOLOGY BRUSH?
The FDA 510(k) record lists Bioteque America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CYTOLOGY BRUSH?
The FDA product code for CYTOLOGY BRUSH is HHT.
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 Bioteque America, 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: HHT)
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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