Acuvance Plus Safety IV Catheter, Protectiv Plus Safety IV Catheter, Optiva IV Catheter

FDA 510(k) K030571 · Ethicon Endo-Surgery, Inc.

Substantially Equivalent

510(k) numberK030571

Submission

Device name
Acuvance Plus Safety IV Catheter, Protectiv Plus Safety IV Catheter, Optiva IV Catheter
Applicant
Ethicon Endo-Surgery, Inc.
Cincinnati, OH, US
Received
February 24, 2003
Decision date
March 28, 2003
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FOZ – Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5200
Specialty
General Hospital

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K252398SURFLO Hybria Closed System Safety IV CatheterFOZ · Traditional Terumo Medical Products (Hangzhou) Co., Ltd.12/17/2025SE
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Questions and answers

When was Acuvance Plus Safety IV Catheter, Protectiv Plus Safety IV Catheter, Optiva IV Catheter cleared by the FDA?

Acuvance Plus Safety IV Catheter, Protectiv Plus Safety IV Catheter, Optiva IV Catheter (K030571) received a 510(k) decision of Substantially Equivalent on March 28, 2003, 32 days after the submission was received.

What is the product code of K030571?

The FDA product code is FOZ – Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days, a Class II (moderate risk) device regulated under 21 CFR 880.5200.