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FDA 510(k)

Forwarts

K-Number: K201366 · 2021-01-21

ApplicantPronova Laboratories BV
Decision Date2021-01-21
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Forwarts is a medical device manufactured by Pronova Laboratories BV. It received FDA 510(k) clearance on 2021-01-21 under approval number K201366. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Forwarts?

Forwarts is a medical device that received FDA 510(k) clearance on 2021-01-21. It is manufactured by Pronova Laboratories BV. The 510(k) number is K201366.

When was Forwarts approved by the FDA?

Forwarts received FDA 510(k) clearance on 2021-01-21, under approval number K201366.

What company makes Forwarts?

Forwarts is manufactured by Pronova Laboratories BV.

What is the FDA product code for Forwarts?

The FDA product code for Forwarts is GEH.

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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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