Flow Sensors

by Corvent Medical, Inc

Flow Sensors (91-101-US209) 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 00850057117110), active as of 31 May 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 31 May 2026

Documents

FDA submission, from GUDID

Trust

Source GUDID, synced 31 May 2026.

Regulatory status

as of registry sync 31 May 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00850057117110 UDI-DI	Date5 Jun 2025Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK241135	Date13 Nov 2024Decided	StatusActive

Official records

AccessGUDID record UDI-DI 00850057117110
FDA 510(k) database 510(k) number K241135

Across registries

2 registries list this device

FDA 510(k) K241135 decided 13 Nov 2024 Active
FDA GUDID UDI-DI 00850057117110 listed 5 Jun 2025 Listed

Timeline

2 dated events

13 Nov 2024 Cleared FDA 510(k) K241135
5 Jun 2025 Listed FDA GUDID 00850057117110

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Generic name: Breathing circuit gas-flow sensor, reusable
Model / Ref / Catalog: Flow Sensors, 91-101-US209

Primary DI / UDI-DI: 00850057117110
510(k) Number: K241135
FDA product code: CBK
GMDN term: Breathing circuit gas-flow sensor, reusable

Device class: Class II
Regulation number: 868.5895
GUDID distribution status: In Commercial Distribution

Other devices from Corvent Medical, Inc

See all devices from Corvent Medical, Inc →

Properties

Single use
Prescription use
Lot / batch number
Expiration date

Other properties (11, all answered No)