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FDA 510(k)

HORIZON 2000/S 266-XXX-XXX

K-Number: K880595 · 1988-05-06

ApplicantMennen Medical, Inc.
Decision Date1988-05-06
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HORIZON 2000/S 266-XXX-XXX 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 1988-05-06 under 510(k) number K880595. 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/S 266-XXX-XXX?

HORIZON 2000/S 266-XXX-XXX is a medical device that received FDA 510(k) clearance on 1988-05-06. The listed applicant is Mennen Medical, Inc.. The 510(k) number is K880595.

When did HORIZON 2000/S 266-XXX-XXX receive FDA 510(k) clearance?

HORIZON 2000/S 266-XXX-XXX received FDA 510(k) clearance on 1988-05-06, under 510(k) number K880595.

Who is the listed applicant for HORIZON 2000/S 266-XXX-XXX?

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/S 266-XXX-XXX?

The FDA product code for HORIZON 2000/S 266-XXX-XXX 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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