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510(k) K243926

Vivatmo pro-S by Bosch Healthcare Solutions GmbH — Product Code MXA

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 11, 2025
Date Received
December 20, 2024
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Breath Nitric Oxide
Device Class
Class II
Regulation Number
862.3080
Review Panel
CH
Submission Type

Other clearances by Bosch Healthcare Solutions GmbH

  • K233775 — Vivatmo pro (February 22, 2024)

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  • K213611 — Fenom Pro (June 7, 2023)
  • K203695 — NObreath® (December 17, 2021)
  • K182874 — Fenom Pro Nitric Oxide Test (February 13, 2019)
  • K170983 — NIOX VERO (November 22, 2017)
  • K150233 — NIOX VERO Airway Inflammation Monitor (February 26, 2015)
  • K133898 — NIOX VERO AIRWAY INFLAMMATION MONITOR (November 6, 2014)
  • K123683 — NIOX PANEL FOR USE WITH THE NIOX MINO AIRWAY INFLAMMATION MONITOR (December 27, 2012)
  • K101034 — NIOX MINO MODEL 09-1000 (September 2, 2010)