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FDA 510(k)

VENTNET; CENTRAL MONITORING STATION

K-Number: K963633 · 1996-12-16

ApplicantPuritan Bennett Corp.
Decision Date1996-12-16
Product CodeMOD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENTNET; CENTRAL MONITORING STATION is the device name listed in this FDA 510(k) record. The listed applicant is Puritan Bennett Corp.. It received FDA 510(k) clearance on 1996-12-16 under 510(k) number K963633. 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 VENTNET; CENTRAL MONITORING STATION?

VENTNET; CENTRAL MONITORING STATION is a medical device that received FDA 510(k) clearance on 1996-12-16. The listed applicant is Puritan Bennett Corp.. The 510(k) number is K963633.

When did VENTNET; CENTRAL MONITORING STATION receive FDA 510(k) clearance?

VENTNET; CENTRAL MONITORING STATION received FDA 510(k) clearance on 1996-12-16, under 510(k) number K963633.

Who is the listed applicant for VENTNET; CENTRAL MONITORING STATION?

The FDA 510(k) record lists Puritan Bennett Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENTNET; CENTRAL MONITORING STATION?

The FDA product code for VENTNET; CENTRAL MONITORING STATION is MOD.

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Other records listing Puritan Bennett Corp. 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.

K063650VENTILATOR WITH RESPIRATORY MECHANICS, MODEL 840K053388MODEL 840 VENTILATOR WITH PROPORTIONAL ASSIST VENTILATION PLUS SOFTWARE OPTIONK023225PURITAN BENNETT DATAFLOW DATA MANAGEMENT SOFTWAREK022103PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEMK001646PURITAN-BENNETT 840 VENTILATOR SYSTEM WITH NEOMODE OPTIONK002001BREEZE SLEEPGEAR WITH DREAMSEAL

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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

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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