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FDA 510(k)

CYCLO-BRUSH

K-Number: K870782 · 1987-05-18

ApplicantMedline Industries, Inc.
Decision Date1987-05-18
Product CodeHHT
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CYCLO-BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1987-05-18 under 510(k) number K870782. The device is classified under product code HHT. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYCLO-BRUSH?

CYCLO-BRUSH is a medical device that received FDA 510(k) clearance on 1987-05-18. The listed applicant is Medline Industries, Inc.. The 510(k) number is K870782.

When did CYCLO-BRUSH receive FDA 510(k) clearance?

CYCLO-BRUSH received FDA 510(k) clearance on 1987-05-18, under 510(k) number K870782.

Who is the listed applicant for CYCLO-BRUSH?

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

What is the FDA product code for CYCLO-BRUSH?

The FDA product code for CYCLO-BRUSH is HHT.

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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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