FDA 510(k)

F5 Corpus VS

K-Number: K191874 · 2019-10-25

Decision Date2019-10-25

Product CodeIPL

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

F5 Corpus VS is the device name listed in this FDA 510(k) record. The listed applicant is Permobil AB. It received FDA 510(k) clearance on 2019-10-25 under 510(k) number K191874. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the F5 Corpus VS?

F5 Corpus VS is a medical device that received FDA 510(k) clearance on 2019-10-25. The listed applicant is Permobil AB. The 510(k) number is K191874.

When did F5 Corpus VS receive FDA 510(k) clearance?

F5 Corpus VS received FDA 510(k) clearance on 2019-10-25, under 510(k) number K191874.

Who is the listed applicant for F5 Corpus VS?

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

What is the FDA product code for F5 Corpus VS?

The FDA product code for F5 Corpus VS is IPL.

Other records listing Permobil AB 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.

K190682Explorer Mini

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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.