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FDA 510(k)

NEOPIP PATIENT CIRCUIT WITH PEEP

K-Number: K103833 · 2011-04-20

ApplicantNeoforce Group, Inc.
Decision Date2011-04-20
Product CodeBYE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEOPIP PATIENT CIRCUIT WITH PEEP is the device name listed in this FDA 510(k) record. The listed applicant is Neoforce Group, Inc.. It received FDA 510(k) clearance on 2011-04-20 under 510(k) number K103833. The device is classified under product code BYE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEOPIP PATIENT CIRCUIT WITH PEEP?

NEOPIP PATIENT CIRCUIT WITH PEEP is a medical device that received FDA 510(k) clearance on 2011-04-20. The listed applicant is Neoforce Group, Inc.. The 510(k) number is K103833.

When did NEOPIP PATIENT CIRCUIT WITH PEEP receive FDA 510(k) clearance?

NEOPIP PATIENT CIRCUIT WITH PEEP received FDA 510(k) clearance on 2011-04-20, under 510(k) number K103833.

Who is the listed applicant for NEOPIP PATIENT CIRCUIT WITH PEEP?

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

What is the FDA product code for NEOPIP PATIENT CIRCUIT WITH PEEP?

The FDA product code for NEOPIP PATIENT CIRCUIT WITH PEEP is BYE.

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Other records listing Neoforce Group, 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.

K110119PRESSURE MANOMETERK102649NEOPOP INFANT RESUSCITATOR WITH FLOW METERK092085ISPIRA RESUSCITATION UNITK072021NEOPIP INFANT RESUSCITATORK070416NEOPEEP NEONATAL RESUSCITATION CIRCUIT WITH PEEPK061280V-2200 INFANT INCUBATOR

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Related Devices (Code: BYE)

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.

K160112Besmed PEEP ValveBesmed Health Business CorpK122610PLAXTRON CPAP SYSTEM, MODEL CH-FFM-87XX/CH-FFM-88XX SERIESSen MU Technology Co., Ltd.K112546O_TWO CPAP SYSTEMO-Two Medical Technologies, Inc.K110713WATERPAP VALVEAirways Development, LLCK092029VENTSTAR RESUSCITAIRE, MODEL MP00311, VENTSTAR RESUSCITAIRE CEU, MODEL MP00310Draeger Medical AG & Co. KGK090710MERCURY CPAPMercury Medical

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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