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FDA 510(k)

F5 Corpus VS

K-Number: K191874 · 2019-10-25

ApplicantPermobil AB
Decision Date2019-10-25
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

F5 Corpus VS is a medical device manufactured by Permobil AB. It received FDA 510(k) clearance on 2019-10-25 under approval 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. It is manufactured by Permobil AB. The 510(k) number is K191874.

When was F5 Corpus VS approved by the FDA?

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

What company makes F5 Corpus VS?

F5 Corpus VS is manufactured by Permobil AB.

What is the FDA product code for F5 Corpus VS?

The FDA product code for F5 Corpus VS is IPL.

Other Devices by Permobil AB

K190682Explorer Mini

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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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