Protectiv Acuvance IV Catheter System

FDA 510(k) K012128 · Ethicon Endo-Surgery, Inc.

Substantially Equivalent

510(k) numberK012128

Submission

Device name
Protectiv Acuvance IV Catheter System
Applicant
Ethicon Endo-Surgery, Inc.
Cincinnati, OH, US
Received
July 9, 2001
Decision date
August 1, 2001
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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K253235Introcan Safety® Deep Access XL IV CatheterFOZ · Traditional B.Braun Medical, Inc.05/15/2026SE
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K252513Polywin Safety (14G x 51mm; 16G x 51mm; 18G x 64mm; 20G x 64mm; 20G x 45mm; 22G x 64mm…FOZ · Special Poly Medicure Limited04/01/2026SE
K252398SURFLO Hybria Closed System Safety IV CatheterFOZ · Traditional Terumo Medical Products (Hangzhou) Co., Ltd.12/17/2025SE
K252677Polyshield Safety IV CathetersFOZ · Special Poly Medicure Limited11/05/2025SE
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K230387ENSEAL X1 Curved Tissue Sealers, 25 cm shaft length (NSLX125C); ENSEAL X1 Curved Tissue…GEI · Traditional 04/13/2023SE
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Questions and answers

When was Protectiv Acuvance IV Catheter System cleared by the FDA?

Protectiv Acuvance IV Catheter System (K012128) received a 510(k) decision of Substantially Equivalent on August 1, 2001, 23 days after the submission was received.

What is the product code of K012128?

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.