Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00620); Arrow Endurance Extended Dwell Peripheral Cathete
Summary
Arrow International, LLC (A subsidiary of Teleflex, Inc.) received 510(k) clearance for Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00620); Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00622); Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00820); Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00822), a FOZ device. Cleared on 2024-12-20.
Details
Source
510(k) Clearance
External ID
K242281
Action Date
2024-12-20
Status
Traditional
Category
device
Product Code
FOZ
Product Description
Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00620); Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00622); Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00820); Arrow Endurance Extended Dwell Peripheral Catheter System (EDC-00822). Product code: FOZ.
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Arrow International, LLC (A subsidiary of Teleflex, Inc.) has received 4 total clearances in our database.
Arrow International, LLC (A subsidiary of Teleflex, Inc.) has 4 FDA actions in our database, including 4 clearances.
Frequently Asked Questions
What does 510(k) clearance mean?
A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.
How often does Arrow International, LLC (A subsidiary of Teleflex, Inc.) have FDA actions?
Arrow International, LLC (A subsidiary of Teleflex, Inc.) has 4 FDA actions in our database, including 0 recalls and 4 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K242281" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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