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FDA 510(k)

PULSED OXYGEN CONSERVING DEVICE, POCD

K-Number: K983459 · 1998-12-08

ApplicantMedical Electronic Devices, Inc.
Decision Date1998-12-08
Product CodeNFB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PULSED OXYGEN CONSERVING DEVICE, POCD is the device name listed in this FDA 510(k) record. The listed applicant is Medical Electronic Devices, Inc.. It received FDA 510(k) clearance on 1998-12-08 under 510(k) number K983459. The device is classified under product code NFB. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PULSED OXYGEN CONSERVING DEVICE, POCD?

PULSED OXYGEN CONSERVING DEVICE, POCD is a medical device that received FDA 510(k) clearance on 1998-12-08. The listed applicant is Medical Electronic Devices, Inc.. The 510(k) number is K983459.

When did PULSED OXYGEN CONSERVING DEVICE, POCD receive FDA 510(k) clearance?

PULSED OXYGEN CONSERVING DEVICE, POCD received FDA 510(k) clearance on 1998-12-08, under 510(k) number K983459.

Who is the listed applicant for PULSED OXYGEN CONSERVING DEVICE, POCD?

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

What is the FDA product code for PULSED OXYGEN CONSERVING DEVICE, POCD?

The FDA product code for PULSED OXYGEN CONSERVING DEVICE, POCD is NFB.

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Other records listing Medical Electronic Devices, 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.

K052563INOGEN SATELLITE CONSERVER, MODEL SC-100K033197INOGEN SATELLITE CONSERVERK023420PULSED OXYGEN CONSERVING DEVICE - EVERY BREATH, POCDEB, REACTEBK983601DEMAND OXYGEN CONSERVING DEVICE, DOCD, THE DOCK770115ARTERIAL DIAGNOSTIC UNIT (ADU)K761092INGUINAL COMPRESSIVE DEVICE (ICD)

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Related Devices (Code: NFB)

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.

K250322Respond OC Conserving Regulator (130-0800)Responsive RespiratoryK220591ProximaDynasthetics, LLCK221014Effortless Oxygen Conserver System Models Effortless Pro and Effortless MobileEffortless Oxygen, LLCK200401ApogeeIncoba Ltd D/B/A DynarisK151506Demand Nasal Oxygen Cannula, Modified Demand Nasal Oxygen CannulaSalter LabsK131023THERAFLOW SINGLE LUMEN AND THERAFLOW DUAL LUMENMedical Products, LLC

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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