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FDA 510(k)

VENTLINK SYSTEM

K-Number: K052751 · 2005-12-23

ApplicantMediserve Information Systems, Inc.
Decision Date2005-12-23
Product CodeMOD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENTLINK SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Mediserve Information Systems, Inc.. It received FDA 510(k) clearance on 2005-12-23 under 510(k) number K052751. The device is classified under product code MOD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTLINK SYSTEM?

VENTLINK SYSTEM is a medical device that received FDA 510(k) clearance on 2005-12-23. The listed applicant is Mediserve Information Systems, Inc.. The 510(k) number is K052751.

When did VENTLINK SYSTEM receive FDA 510(k) clearance?

VENTLINK SYSTEM received FDA 510(k) clearance on 2005-12-23, under 510(k) number K052751.

Who is the listed applicant for VENTLINK SYSTEM?

The FDA 510(k) record lists Mediserve Information Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENTLINK SYSTEM?

The FDA product code for VENTLINK SYSTEM is MOD.

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Related Devices (Code: MOD)

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.

K261360EasyCare Tx 2Resmed CorpK253807Valence InVent Xtend™ (CVG-4101-VXA)Convergence Medical Sciences , Ltd.K260051CorVision® (91-205-Z0014)CorVent® Medical, Inc.K242485EveryWareBreas Medical ABK161411Care Cycle Connect ApplicationRespironics, Inc.K091461BERNOULLI MANAGEMENT SYSTEM, OXINET III AND LIFEGARD VUECardiopulmonary Corp.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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