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FDA 510(k)

AKUPORT M-2

K-Number: K020568 · 2002-04-30

ApplicantVibrant Health
Decision Date2002-04-30
Product CodeGZO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AKUPORT M-2 is the device name listed in this FDA 510(k) record. The listed applicant is Vibrant Health. It received FDA 510(k) clearance on 2002-04-30 under 510(k) number K020568. 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 M-2?

AKUPORT M-2 is a medical device that received FDA 510(k) clearance on 2002-04-30. The listed applicant is Vibrant Health. The 510(k) number is K020568.

When did AKUPORT M-2 receive FDA 510(k) clearance?

AKUPORT M-2 received FDA 510(k) clearance on 2002-04-30, under 510(k) number K020568.

Who is the listed applicant for AKUPORT M-2?

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 M-2?

The FDA product code for AKUPORT M-2 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.

K020567AKUPORT M1K020565EAV COMBI-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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