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FDA 510(k)

HORIZON 2000 ST ANALYSIS OPTION

K-Number: K903524 · 1991-03-01

ApplicantMennen Medical, Inc.
Decision Date1991-03-01
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HORIZON 2000 ST ANALYSIS OPTION 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 1991-03-01 under 510(k) number K903524. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HORIZON 2000 ST ANALYSIS OPTION?

HORIZON 2000 ST ANALYSIS OPTION is a medical device that received FDA 510(k) clearance on 1991-03-01. The listed applicant is Mennen Medical, Inc.. The 510(k) number is K903524.

When did HORIZON 2000 ST ANALYSIS OPTION receive FDA 510(k) clearance?

HORIZON 2000 ST ANALYSIS OPTION received FDA 510(k) clearance on 1991-03-01, under 510(k) number K903524.

Who is the listed applicant for HORIZON 2000 ST ANALYSIS OPTION?

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 2000 ST ANALYSIS OPTION?

The FDA product code for HORIZON 2000 ST ANALYSIS OPTION is DPS.

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Other records listing Mennen Medical, Inc. as applicant

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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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