FDA.report

510(k) K222341

Device
Arrow 0.2 Micron Flat Filter, GVS
Applicant
Arrow International, LLC
510(k) number
K222341
Product code
CAZ
Decision
Substantially Equivalent (SESE)
Decision date
2023-02-13
Date received
2022-08-03
Regulation
868.5140
Classification name
Anesthesia Conduction Kit
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Ann Metz
Address
3015 Carrington Mill Blvd. Morrisville NC US 27560 27560

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
20801902214014ARROWTELEFLEX INCORPORATED2023-07-22

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