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FDA 510(k)

HORIZON 2000 NON-INVASIVE BLOOD PRESSURE CAP.

K-Number: K854942 · 1986-06-02

ApplicantMennen Medical, Inc.
Decision Date1986-06-02
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HORIZON 2000 NON-INVASIVE BLOOD PRESSURE CAP. 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 1986-06-02 under 510(k) number K854942. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HORIZON 2000 NON-INVASIVE BLOOD PRESSURE CAP.?

HORIZON 2000 NON-INVASIVE BLOOD PRESSURE CAP. is a medical device that received FDA 510(k) clearance on 1986-06-02. The listed applicant is Mennen Medical, Inc.. The 510(k) number is K854942.

When did HORIZON 2000 NON-INVASIVE BLOOD PRESSURE CAP. receive FDA 510(k) clearance?

HORIZON 2000 NON-INVASIVE BLOOD PRESSURE CAP. received FDA 510(k) clearance on 1986-06-02, under 510(k) number K854942.

Who is the listed applicant for HORIZON 2000 NON-INVASIVE BLOOD PRESSURE CAP.?

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 NON-INVASIVE BLOOD PRESSURE CAP.?

The FDA product code for HORIZON 2000 NON-INVASIVE BLOOD PRESSURE CAP. is DXN.

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Related Devices (Code: DXN)

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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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