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FDA 510(k)

PULSED OXYGEN CONSERVING DEVICE - EVERY BREATH, POCDEB, REACTEB

K-Number: K023420 · 2002-10-25

ApplicantMedical Electronic Devices, Inc.
Decision Date2002-10-25
Product CodeNFB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PULSED OXYGEN CONSERVING DEVICE - EVERY BREATH, POCDEB, REACTEB 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 2002-10-25 under 510(k) number K023420. 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 - EVERY BREATH, POCDEB, REACTEB?

PULSED OXYGEN CONSERVING DEVICE - EVERY BREATH, POCDEB, REACTEB is a medical device that received FDA 510(k) clearance on 2002-10-25. The listed applicant is Medical Electronic Devices, Inc.. The 510(k) number is K023420.

When did PULSED OXYGEN CONSERVING DEVICE - EVERY BREATH, POCDEB, REACTEB receive FDA 510(k) clearance?

PULSED OXYGEN CONSERVING DEVICE - EVERY BREATH, POCDEB, REACTEB received FDA 510(k) clearance on 2002-10-25, under 510(k) number K023420.

Who is the listed applicant for PULSED OXYGEN CONSERVING DEVICE - EVERY BREATH, POCDEB, REACTEB?

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 - EVERY BREATH, POCDEB, REACTEB?

The FDA product code for PULSED OXYGEN CONSERVING DEVICE - EVERY BREATH, POCDEB, REACTEB 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.

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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.

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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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