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FDA 510(k)

ANSHA AUTONOMIC NERVOUS SYSTEM HEALTH ASSESSMENT PLUS

K-Number: K083735 · 2009-02-18

ApplicantMedtechs, LLC
Decision Date2009-02-18
Product CodeJOM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANSHA AUTONOMIC NERVOUS SYSTEM HEALTH ASSESSMENT PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Medtechs, LLC. It received FDA 510(k) clearance on 2009-02-18 under 510(k) number K083735. The device is classified under product code JOM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANSHA AUTONOMIC NERVOUS SYSTEM HEALTH ASSESSMENT PLUS?

ANSHA AUTONOMIC NERVOUS SYSTEM HEALTH ASSESSMENT PLUS is a medical device that received FDA 510(k) clearance on 2009-02-18. The listed applicant is Medtechs, LLC. The 510(k) number is K083735.

When did ANSHA AUTONOMIC NERVOUS SYSTEM HEALTH ASSESSMENT PLUS receive FDA 510(k) clearance?

ANSHA AUTONOMIC NERVOUS SYSTEM HEALTH ASSESSMENT PLUS received FDA 510(k) clearance on 2009-02-18, under 510(k) number K083735.

Who is the listed applicant for ANSHA AUTONOMIC NERVOUS SYSTEM HEALTH ASSESSMENT PLUS?

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

What is the FDA product code for ANSHA AUTONOMIC NERVOUS SYSTEM HEALTH ASSESSMENT PLUS?

The FDA product code for ANSHA AUTONOMIC NERVOUS SYSTEM HEALTH ASSESSMENT PLUS is JOM.

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.

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Other records listing Medtechs, LLC 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.

K080884QHRV 1 - HEALTH ASSESSMENT SYSTEM

Related Devices (Code: JOM)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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