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FDA 510(k)

PAT (Pain Alleviation Technologies)

K-Number: K182267 · 2019-02-27

ApplicantMarchan Medical, LLC
Decision Date2019-02-27
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PAT (Pain Alleviation Technologies) is the device name listed in this FDA 510(k) record. The listed applicant is Marchan Medical, LLC. It received FDA 510(k) clearance on 2019-02-27 under 510(k) number K182267. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAT (Pain Alleviation Technologies)?

PAT (Pain Alleviation Technologies) is a medical device that received FDA 510(k) clearance on 2019-02-27. The listed applicant is Marchan Medical, LLC. The 510(k) number is K182267.

When did PAT (Pain Alleviation Technologies) receive FDA 510(k) clearance?

PAT (Pain Alleviation Technologies) received FDA 510(k) clearance on 2019-02-27, under 510(k) number K182267.

Who is the listed applicant for PAT (Pain Alleviation Technologies)?

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

What is the FDA product code for PAT (Pain Alleviation Technologies)?

The FDA product code for PAT (Pain Alleviation Technologies) is NUH.

Related Devices (Code: NUH)

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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