MICROBIOLOGY SPECIMEN BRUSH
K-Number: K820771 · 1982-05-03
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Device Summary
Frequently Asked Questions
What is the MICROBIOLOGY SPECIMEN BRUSH?
MICROBIOLOGY SPECIMEN BRUSH is a medical device that received FDA 510(k) clearance on 1982-05-03. The listed applicant is Mill-Rose Laboratory. The 510(k) number is K820771.
When did MICROBIOLOGY SPECIMEN BRUSH receive FDA 510(k) clearance?
MICROBIOLOGY SPECIMEN BRUSH received FDA 510(k) clearance on 1982-05-03, under 510(k) number K820771.
Who is the listed applicant for MICROBIOLOGY SPECIMEN BRUSH?
The FDA 510(k) record lists Mill-Rose Laboratory as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROBIOLOGY SPECIMEN BRUSH?
The FDA product code for MICROBIOLOGY SPECIMEN BRUSH is BTG.
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 Mill-Rose Laboratory 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: BTG)
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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