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FDA 510(k)

P.E.E.P. VALVE

K-Number: K882219 · 1988-08-30

ApplicantLife Support Products, Inc.
Decision Date1988-08-30
Product CodeBYE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

P.E.E.P. VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Life Support Products, Inc.. It received FDA 510(k) clearance on 1988-08-30 under 510(k) number K882219. 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 P.E.E.P. VALVE?

P.E.E.P. VALVE is a medical device that received FDA 510(k) clearance on 1988-08-30. The listed applicant is Life Support Products, Inc.. The 510(k) number is K882219.

When did P.E.E.P. VALVE receive FDA 510(k) clearance?

P.E.E.P. VALVE received FDA 510(k) clearance on 1988-08-30, under 510(k) number K882219.

Who is the listed applicant for P.E.E.P. VALVE?

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

What is the FDA product code for P.E.E.P. VALVE?

The FDA product code for P.E.E.P. VALVE is BYE.

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Other records listing Life Support Products, 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.

K941870LSPI AUTOMATIC VENTILATOR, MODEL AV2000-100K941871LSPI AUTOMATIC VENTILATOR, MODEL AV3000-100K940934LIFE VACK936187LSPI PRESSURE REGULATORK932199LSPI AUTOMATIC VENTILATOR, MODEL AV3000K922691LSP (MODEL 554) BAG MASK RESUSCITATOR

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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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