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FDA 510(k)

COPD LIQUID OXYGEN PORTABLE, MODEL 300P

K-Number: K072011 · 2007-10-18

ApplicantCopd Partners, Inc.
Decision Date2007-10-18
Product CodeBYJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COPD LIQUID OXYGEN PORTABLE, MODEL 300P is the device name listed in this FDA 510(k) record. The listed applicant is Copd Partners, Inc.. It received FDA 510(k) clearance on 2007-10-18 under 510(k) number K072011. The device is classified under product code BYJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COPD LIQUID OXYGEN PORTABLE, MODEL 300P?

COPD LIQUID OXYGEN PORTABLE, MODEL 300P is a medical device that received FDA 510(k) clearance on 2007-10-18. The listed applicant is Copd Partners, Inc.. The 510(k) number is K072011.

When did COPD LIQUID OXYGEN PORTABLE, MODEL 300P receive FDA 510(k) clearance?

COPD LIQUID OXYGEN PORTABLE, MODEL 300P received FDA 510(k) clearance on 2007-10-18, under 510(k) number K072011.

Who is the listed applicant for COPD LIQUID OXYGEN PORTABLE, MODEL 300P?

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

What is the FDA product code for COPD LIQUID OXYGEN PORTABLE, MODEL 300P?

The FDA product code for COPD LIQUID OXYGEN PORTABLE, MODEL 300P is BYJ.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Copd Partners, 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.

K071461MODEL 300D HOME OXYGEN LIQUEFIER

Related Devices (Code: BYJ)

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.

K130068DISMOUNTED MEDICAL & SUPPLEMENTAL OXYGEN SYSTEM (DMOS)Essex Industries, Inc. D/B/A Essex Cryogenics of MK113767MOUNTED MEDICAL OXYGEN SYSTEMEssex Industries, Inc.K103324PRECISION LIQUID OXYGEN SYSTEMPrecision Medical, Inc.K101272MASS OXYGEN DISTRIBUTION SYSTEM (MODS) MODEL 10C-0061-3Essex Industries, Inc.K081779GOLOX-93Respironics, Inc.K080023MODIFICATION TO: SPIRITCaire, Inc.

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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