DeviceSignal · 510(k) cleared

Mozarc Medical Us, LLC

FDA 510(k) decision recorded 2026-08-06 · K253469 · Traditional 510(k)

Event510(k) cleared
Effective2026-08-06
DecisionSESE

On 2026-08-06 the FDA recorded a 510(k) clearance decision for Mozarc Medical Us, LLC, for Ritus™ Safety Fistula Cannula with Anti-Reflux Valve 15G x 30mm (1530VSMM); Ritus™ Safety…. Clearance K253469. Product code FIE. A clearance is a regulatory decision, not an endorsement of the device.

Reported facts

510(k) number
K253469
Applicant
Mozarc Medical Us, LLC
Device
Ritus™ Safety Fistula Cannula with Anti-Reflux Valve 15G x 30mm (1530VSMM); Ritus™ Safety Fistula Cannula with Anti-Reflux Valve 15G x 38mm (1538VSMM); Ritus™ Safety Fistula Cannula with Anti-Reflux Valve 16G x 30mm (1630VSMM); Ritus™ Safety Fistula Cannula with Anti-Reflux Valve 16G x 38mm (1638VSMM); Ritus™ Safety Fistula Cannula with Anti-Reflux Valve 17G x 30mm (1730VSMM); Ritus™ Safety Fistula Cannula with Anti-Reflux Valve 17G x 38mm (1738VSMM)
Decided on
2026-08-06
Received on
2025-10-10
Decision
SESE
Clearance type
Traditional
Product code
FIE
Review days
300

Every field above is as fda_device_510k published it. Nothing on this page is our interpretation.

Provenance

Source
fda_device_510k
Source record
K253469
Snapshot hash
a17b676375c92ad46cfd0c81b2c18852150764f05c544c0889e193548d652e00
Source URL
https://download.open.fda.gov/device/510k/device-510k-0001-of-0001.json.zip
Observed
2026-09-08T16:22:09.483Z
Transform
fda_device_510k_to_clearance v1
Event rule
fda_device_510k_cleared v1
Event key
99357fef67a670e9b88d09ffc3da0e9b81c5d36e44c938dbf781c403f2e57f7c
Signal type
device_clearance.granted

Source terms that apply

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Data provided by the U.S. Food and Drug Administration (https://open.fda.gov)