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FDA 510(k)

HORIZON DISPLAY CONTROLLER PART # 266-200-010

K-Number: K884423 · 1989-05-31

ApplicantMennen Medical, Inc.
Decision Date1989-05-31
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HORIZON DISPLAY CONTROLLER PART # 266-200-010 is the device name listed in this FDA 510(k) record. The listed applicant is Mennen Medical, Inc.. It received FDA 510(k) clearance on 1989-05-31 under 510(k) number K884423. The device is classified under product code DXJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HORIZON DISPLAY CONTROLLER PART # 266-200-010?

HORIZON DISPLAY CONTROLLER PART # 266-200-010 is a medical device that received FDA 510(k) clearance on 1989-05-31. The listed applicant is Mennen Medical, Inc.. The 510(k) number is K884423.

When did HORIZON DISPLAY CONTROLLER PART # 266-200-010 receive FDA 510(k) clearance?

HORIZON DISPLAY CONTROLLER PART # 266-200-010 received FDA 510(k) clearance on 1989-05-31, under 510(k) number K884423.

Who is the listed applicant for HORIZON DISPLAY CONTROLLER PART # 266-200-010?

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

What is the FDA product code for HORIZON DISPLAY CONTROLLER PART # 266-200-010?

The FDA product code for HORIZON DISPLAY CONTROLLER PART # 266-200-010 is DXJ.

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Related Devices (Code: DXJ)

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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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