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FDA 510(k)

CLEAN-FLUSH

K-Number: K830572 · 1983-03-17

ApplicantBurron Medical Products, Inc.
Decision Date1983-03-17
Product CodeKYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CLEAN-FLUSH is the device name listed in this FDA 510(k) record. The listed applicant is Burron Medical Products, Inc.. It received FDA 510(k) clearance on 1983-03-17 under 510(k) number K830572. The device is classified under product code KYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEAN-FLUSH?

CLEAN-FLUSH is a medical device that received FDA 510(k) clearance on 1983-03-17. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K830572.

When did CLEAN-FLUSH receive FDA 510(k) clearance?

CLEAN-FLUSH received FDA 510(k) clearance on 1983-03-17, under 510(k) number K830572.

Who is the listed applicant for CLEAN-FLUSH?

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

What is the FDA product code for CLEAN-FLUSH?

The FDA product code for CLEAN-FLUSH is KYZ.

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Related Devices (Code: KYZ)

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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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