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FDA 510(k)

NEOPEEP NEONATAL RESUSCITATION CIRCUIT WITH PEEP

K-Number: K070416 · 2007-05-29

ApplicantNeoforce Group, Inc.
Decision Date2007-05-29
Product CodeBYE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEOPEEP NEONATAL RESUSCITATION 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 2007-05-29 under 510(k) number K070416. 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 NEOPEEP NEONATAL RESUSCITATION CIRCUIT WITH PEEP?

NEOPEEP NEONATAL RESUSCITATION CIRCUIT WITH PEEP is a medical device that received FDA 510(k) clearance on 2007-05-29. The listed applicant is Neoforce Group, Inc.. The 510(k) number is K070416.

When did NEOPEEP NEONATAL RESUSCITATION CIRCUIT WITH PEEP receive FDA 510(k) clearance?

NEOPEEP NEONATAL RESUSCITATION CIRCUIT WITH PEEP received FDA 510(k) clearance on 2007-05-29, under 510(k) number K070416.

Who is the listed applicant for NEOPEEP NEONATAL RESUSCITATION 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 NEOPEEP NEONATAL RESUSCITATION CIRCUIT WITH PEEP?

The FDA product code for NEOPEEP NEONATAL RESUSCITATION 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 MANOMETERK103833NEOPIP PATIENT CIRCUIT WITH PEEPK102649NEOPOP INFANT RESUSCITATOR WITH FLOW METERK092085ISPIRA RESUSCITATION UNITK072021NEOPIP INFANT RESUSCITATORK061280V-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, LLCK103833NEOPIP PATIENT CIRCUIT WITH PEEPNeoforce Group, Inc.K092029VENTSTAR RESUSCITAIRE, MODEL MP00311, VENTSTAR RESUSCITAIRE CEU, MODEL MP00310Draeger Medical AG & Co. KG

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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