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FDA 510(k)

MICROBIOLOGY SPECIMEN BRUSH

K-Number: K820771 · 1982-05-03

Decision Date1982-05-03
Product CodeBTG
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MICROBIOLOGY SPECIMEN BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Mill-Rose Laboratory. It received FDA 510(k) clearance on 1982-05-03 under 510(k) number K820771. The device is classified under product code BTG. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 46 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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