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FDA 510(k)

ENDOBRUSH

K-Number: K870177 · 1987-02-19

ApplicantC & S Microinstruments , Ltd.
Decision Date1987-02-19
Product CodeEKS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ENDOBRUSH is the device name listed in this FDA 510(k) record. The listed applicant is C & S Microinstruments , Ltd.. It received FDA 510(k) clearance on 1987-02-19 under 510(k) number K870177. The device is classified under product code EKS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOBRUSH?

ENDOBRUSH is a medical device that received FDA 510(k) clearance on 1987-02-19. The listed applicant is C & S Microinstruments , Ltd.. The 510(k) number is K870177.

When did ENDOBRUSH receive FDA 510(k) clearance?

ENDOBRUSH received FDA 510(k) clearance on 1987-02-19, under 510(k) number K870177.

Who is the listed applicant for ENDOBRUSH?

The FDA 510(k) record lists C & S Microinstruments , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOBRUSH?

The FDA product code for ENDOBRUSH is EKS.

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Related Devices (Code: EKS)

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.

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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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