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FDA 510(k)

P4 PHYSIO

K-Number: K022175 · 2002-09-09

ApplicantValmed Corp.
Decision Date2002-09-09
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

P4 PHYSIO is the device name listed in this FDA 510(k) record. The listed applicant is Valmed Corp.. It received FDA 510(k) clearance on 2002-09-09 under 510(k) number K022175. 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 P4 PHYSIO?

P4 PHYSIO is a medical device that received FDA 510(k) clearance on 2002-09-09. The listed applicant is Valmed Corp.. The 510(k) number is K022175.

When did P4 PHYSIO receive FDA 510(k) clearance?

P4 PHYSIO received FDA 510(k) clearance on 2002-09-09, under 510(k) number K022175.

Who is the listed applicant for P4 PHYSIO?

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

What is the FDA product code for P4 PHYSIO?

The FDA product code for P4 PHYSIO is IPF.

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.

Other records listing Valmed Corp. 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.

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.

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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