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FDA 510(k)

PHOENIX DRAPES WITH MICROBAN

K-Number: K890917 · 1989-08-17

ApplicantPhoenix Medical Technology, Inc.
Decision Date1989-08-17
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PHOENIX DRAPES WITH MICROBAN is the device name listed in this FDA 510(k) record. The listed applicant is Phoenix Medical Technology, Inc.. It received FDA 510(k) clearance on 1989-08-17 under 510(k) number K890917. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOENIX DRAPES WITH MICROBAN?

PHOENIX DRAPES WITH MICROBAN is a medical device that received FDA 510(k) clearance on 1989-08-17. The listed applicant is Phoenix Medical Technology, Inc.. The 510(k) number is K890917.

When did PHOENIX DRAPES WITH MICROBAN receive FDA 510(k) clearance?

PHOENIX DRAPES WITH MICROBAN received FDA 510(k) clearance on 1989-08-17, under 510(k) number K890917.

Who is the listed applicant for PHOENIX DRAPES WITH MICROBAN?

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

What is the FDA product code for PHOENIX DRAPES WITH MICROBAN?

The FDA product code for PHOENIX DRAPES WITH MICROBAN is KGX.

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Other records listing Phoenix Medical Technology, Inc. as applicant

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Related Devices (Code: KGX)

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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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