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NIOX MINO NO Scrubber

by Circassia AB

NIOX MINO NO Scrubber (09-1300) is a nitrogen monoxide analyser (FDA Class II; FDA product code MXA, System,Test,Breath Nitric Oxide) made by Circassia AB, cleared under FDA 510(k) K101034 on 2 Sep 2010 and listed in FDA GUDID since 21 Sep 2016 (UDI-DI 07350047030113), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K101034

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07350047030113 UDI-DI Date21 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK101034 Date2 Sep 2010DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K101034 decided 2 Sep 2010 Active
  • FDA GUDID UDI-DI 07350047030113 listed 21 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K101034
  2. Listed FDA GUDID 07350047030113

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Niox
Generic name
Nitrogen monoxide analyser
Model / Ref / Catalog
MINO NO Scrubber, 09-1300
Primary DI / UDI-DI
07350047030113
510(k) Number
FDA product code
MXA
GMDN term
Nitrogen monoxide analyser
Device class
Class II
Regulation number
862.3080
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code MXA (System,Test,Breath Nitric Oxide).

Other devices from Circassia AB

See all devices from Circassia AB →

Properties

  • Prescription use
  • Serial number
  • Expiration date
Other properties (12, all answered No)