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FDA 510(k)

VITALOGRAPH 2110 SOFTWARE INTERFACE

K-Number: K950854 · 1995-10-12

ApplicantVitalograph , Ltd.
Decision Date1995-10-12
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VITALOGRAPH 2110 SOFTWARE INTERFACE is the device name listed in this FDA 510(k) record. The listed applicant is Vitalograph , Ltd.. It received FDA 510(k) clearance on 1995-10-12 under 510(k) number K950854. The device is classified under product code DSH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITALOGRAPH 2110 SOFTWARE INTERFACE?

VITALOGRAPH 2110 SOFTWARE INTERFACE is a medical device that received FDA 510(k) clearance on 1995-10-12. The listed applicant is Vitalograph , Ltd.. The 510(k) number is K950854.

When did VITALOGRAPH 2110 SOFTWARE INTERFACE receive FDA 510(k) clearance?

VITALOGRAPH 2110 SOFTWARE INTERFACE received FDA 510(k) clearance on 1995-10-12, under 510(k) number K950854.

Who is the listed applicant for VITALOGRAPH 2110 SOFTWARE INTERFACE?

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

What is the FDA product code for VITALOGRAPH 2110 SOFTWARE INTERFACE?

The FDA product code for VITALOGRAPH 2110 SOFTWARE INTERFACE is DSH.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Vitalograph , Ltd. 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.

K253293VitaloJAK Clinic (Model 7100)K925085ESCORT SPIROMETERK930085VITALOGRAPH DATA STORAGE SPIROMETERK912412VITALOGRAPH SPIROTRAC IIIK893665AEROSOL INHALATION MONITORK892524VITALOGRAPH-BREATHCO MONITOR

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Related Devices (Code: DSH)

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.

K260157LifeLens Physiological MonitorLifeLens Technologies, Inc.K252389Rhythm Master ECG Patch (HM-15BB-AX, HM-15BW-AX, HM-15BW-DX)Smwmed, Inc.K253293VitaloJAK Clinic (Model 7100)Vitalograph , Ltd.K243650Zio® monitor (DFG0001)iRhythm Technologies, Inc.K243603AeviceMDAevice Health Pte. , Ltd.K242583AT-Patch (ATP-C130/ATP-C70)Atsens Co., 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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