FDA 510(k)

STERILE CYTOLOGY BRUSHES

K-Number: K820259 · 1982-03-05

Decision Date1982-03-05

Product CodeGEE

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

STERILE CYTOLOGY BRUSHES is the device name listed in this FDA 510(k) record. The listed applicant is American Endoscopy, Inc.. It received FDA 510(k) clearance on 1982-03-05 under 510(k) number K820259. The device is classified under product code GEE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE CYTOLOGY BRUSHES?

STERILE CYTOLOGY BRUSHES is a medical device that received FDA 510(k) clearance on 1982-03-05. The listed applicant is American Endoscopy, Inc.. The 510(k) number is K820259.

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

STERILE CYTOLOGY BRUSHES received FDA 510(k) clearance on 1982-03-05, under 510(k) number K820259.

Who is the listed applicant for STERILE CYTOLOGY BRUSHES?

The FDA 510(k) record lists American Endoscopy, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE CYTOLOGY BRUSHES?

The FDA product code for STERILE CYTOLOGY BRUSHES is GEE.

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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.