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FDA 510(k)

HORIZON CENTRAL STATION

K-Number: K892066 · 1989-06-22

ApplicantMennen Medical, Inc.
Decision Date1989-06-22
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HORIZON CENTRAL STATION 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 1989-06-22 under 510(k) number K892066. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HORIZON CENTRAL STATION?

HORIZON CENTRAL STATION is a medical device that received FDA 510(k) clearance on 1989-06-22. The listed applicant is Mennen Medical, Inc.. The 510(k) number is K892066.

When did HORIZON CENTRAL STATION receive FDA 510(k) clearance?

HORIZON CENTRAL STATION received FDA 510(k) clearance on 1989-06-22, under 510(k) number K892066.

Who is the listed applicant for HORIZON CENTRAL STATION?

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 CENTRAL STATION?

The FDA product code for HORIZON CENTRAL STATION is DRT.

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Other records listing Mennen Medical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K030722ENVOY PATIENT MONITORK983864ETCO2 VITAL SIGNS MODULEK991775MODIFICATION TO COMPUTERIZED CATHETERIZATION LABORATORY - HORIZON 9000 WSK982697MODIFICATION TO ENSEMBLE CENTRAL STATION MONITORK974510ENVOY PATIENT MONITORK970358ENSEMBLE CENTRAL STATION MONITOR

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Related Devices (Code: DRT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K254058DistaSense(TM) (v1)Life Detection TechnologiesK261286The Circadia C300 System (C300)Circadia Health, Inc.K252676The Circadia C300 System (C300)Circadia Health, Inc.K253388Sleepiz One+ (Model 2.5)Sleepiz AGK251364Sleepiz One+ (2.5)Sleepiz AGK234003The Circadia C200 SystemCircadia Technologies, Ltd.

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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