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FDA 510(k)

Vivatmo pro

K-Number: K233775 · 2024-02-22

ApplicantBosch Healthcare Solutions GmbH
Decision Date2024-02-22
Product CodeMXA
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

Vivatmo pro is a medical device manufactured by Bosch Healthcare Solutions GmbH. It received FDA 510(k) clearance on 2024-02-22 under approval number K233775. The device is classified under product code MXA. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vivatmo pro?

Vivatmo pro is a medical device that received FDA 510(k) clearance on 2024-02-22. It is manufactured by Bosch Healthcare Solutions GmbH. The 510(k) number is K233775.

When was Vivatmo pro approved by the FDA?

Vivatmo pro received FDA 510(k) clearance on 2024-02-22, under approval number K233775.

What company makes Vivatmo pro?

Vivatmo pro is manufactured by Bosch Healthcare Solutions GmbH.

What is the FDA product code for Vivatmo pro?

The FDA product code for Vivatmo pro is MXA.

Other Devices by Bosch Healthcare Solutions GmbH

K243926Vivatmo pro-S

Related Devices (Code: MXA)

K170983NIOX VEROCircassia AB K182874Fenom Pro Nitric Oxide TestSpirosure, Inc. K203695NObreath®Bedfont Scientific, Ltd. K213611Fenom ProCaire Diagnostics, Inc. K251674Fenom Flo™ FeNO Monitoring SystemMgc Diagnostics Corporation K243926Vivatmo pro-SBosch Healthcare Solutions GmbH

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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