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Circuit Arm

by Corvent Medical, Inc

Circuit Arm (91-101-US308) is a Class II device made by Corvent Medical, Inc, cleared under FDA 510(k) K241135 on 13 Nov 2024 and listed in FDA GUDID since 5 Jun 2025 (UDI-DI 00850057117219), active as of 1 Jun 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 1 Jun 2026

Documents

510(k) K241135

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 1 Jun 2026.

Regulatory status

as of registry sync 1 Jun 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850057117219 UDI-DI Date5 Jun 2025ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK241135 Date13 Nov 2024DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K241135 decided 13 Nov 2024 Active
  • FDA GUDID UDI-DI 00850057117219 listed 5 Jun 2025 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K241135
  2. Listed FDA GUDID 00850057117219

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Generic name
Breathing circuit tube holder
Model / Ref / Catalog
Circuit Arm, 91-101-US308
Primary DI / UDI-DI
00850057117219
510(k) Number
FDA product code
CBK
GMDN term
Breathing circuit tube holder
Device class
Class II
Regulation number
868.5895
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code CBK (Ventilator, Continuous, Facility Use).

Other devices from Corvent Medical, Inc

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  • Exhalation Valve

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See all devices from Corvent Medical, Inc →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)