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FDA 510(k)

Physiq

K-Number: K202079 · 2020-11-25

ApplicantEl.En Electronic Engineering Spa
Decision Date2020-11-25
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Physiq is the device name listed in this FDA 510(k) record. The listed applicant is El.En Electronic Engineering Spa. It received FDA 510(k) clearance on 2020-11-25 under 510(k) number K202079. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Physiq?

Physiq is a medical device that received FDA 510(k) clearance on 2020-11-25. The listed applicant is El.En Electronic Engineering Spa. The 510(k) number is K202079.

When did Physiq receive FDA 510(k) clearance?

Physiq received FDA 510(k) clearance on 2020-11-25, under 510(k) number K202079.

Who is the listed applicant for Physiq?

The FDA 510(k) record lists El.En Electronic Engineering Spa as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Physiq?

The FDA product code for Physiq is IPF.

Other records listing El.En Electronic Engineering Spa as applicant

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Related Devices (Code: IPF)

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

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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