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FDA 510(k)

STERILE DISPOSABLE CYTOLOGY BRUSH

K-Number: K802187 · 1980-09-10

ApplicantOlympus Corp.
Decision Date1980-09-10
Product Code
DecisionUnknown

Device Summary

STERILE DISPOSABLE CYTOLOGY BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1980-09-10 under 510(k) number K802187. FDA Decision: Unknown.

Frequently Asked Questions

What is the STERILE DISPOSABLE CYTOLOGY BRUSH?

STERILE DISPOSABLE CYTOLOGY BRUSH is a medical device that received FDA 510(k) clearance on 1980-09-10. The listed applicant is Olympus Corp.. The 510(k) number is K802187.

When did STERILE DISPOSABLE CYTOLOGY BRUSH receive FDA 510(k) clearance?

STERILE DISPOSABLE CYTOLOGY BRUSH received FDA 510(k) clearance on 1980-09-10, under 510(k) number K802187.

Who is the listed applicant for STERILE DISPOSABLE CYTOLOGY BRUSH?

The FDA 510(k) record lists Olympus Corp. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Olympus Corp. 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.

K915402EW-10 AND EW-20K933200OLYMPUS PBD STENTSK942338OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIESK931763HF-RESECTION ELECTRODE, LOOP W/RUNNER ENDOS/ACCESSK934835FLOVALK931764HF RESECTION ELECTRODE, LOOP W/RUNNER HYSTER/ACCES

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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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