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FDA 510(k)

AKUPORT M1

K-Number: K020567 · 2002-05-02

ApplicantVibrant Health
Decision Date2002-05-02
Product CodeGZO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AKUPORT M1 is the device name listed in this FDA 510(k) record. The listed applicant is Vibrant Health. It received FDA 510(k) clearance on 2002-05-02 under 510(k) number K020567. The device is classified under product code GZO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AKUPORT M1?

AKUPORT M1 is a medical device that received FDA 510(k) clearance on 2002-05-02. The listed applicant is Vibrant Health. The 510(k) number is K020567.

When did AKUPORT M1 receive FDA 510(k) clearance?

AKUPORT M1 received FDA 510(k) clearance on 2002-05-02, under 510(k) number K020567.

Who is the listed applicant for AKUPORT M1?

The FDA 510(k) record lists Vibrant Health as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AKUPORT M1?

The FDA product code for AKUPORT M1 is GZO.

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 Vibrant Health 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.

K020565EAV COMBI-2K020568AKUPORT M-2

Related Devices (Code: GZO)

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.

K131568SUDO PATHLd Technology, LLCK111308ZYTO HAND CRADLEZyto Technologies, Inc.K102166ELECTRO INTERSTITIAL SCANLd Technology, LLCK100233SUDOSCANImpeto MedicalK053004MSAS-VANTAGEBiomeridian, Int.K032935EPI-SCAN, MODEL P 100Edx Epi-Scan, 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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