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FDA 510(k)

Apolo D / Apolo S

K-Number: K202388 · 2020-12-01

ApplicantVmi Tecnologias Ltda
Decision Date2020-12-01
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Apolo D / Apolo S is a medical device manufactured by Vmi Tecnologias Ltda. It received FDA 510(k) clearance on 2020-12-01 under approval number K202388. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Apolo D / Apolo S?

Apolo D / Apolo S is a medical device that received FDA 510(k) clearance on 2020-12-01. It is manufactured by Vmi Tecnologias Ltda. The 510(k) number is K202388.

When was Apolo D / Apolo S approved by the FDA?

Apolo D / Apolo S received FDA 510(k) clearance on 2020-12-01, under approval number K202388.

What company makes Apolo D / Apolo S?

Apolo D / Apolo S is manufactured by Vmi Tecnologias Ltda.

What is the FDA product code for Apolo D / Apolo S?

The FDA product code for Apolo D / Apolo S is KPR.

Other Devices by Vmi Tecnologias Ltda

K201340AQUILA 320 D / AQUILA 320 S K210151Digimamo D

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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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