510(k) K243458

Device
HydroPICC 4Fr Single Lumen Marked catheter, 130 cm guidewire - Basic Kit (70001301); HydroPICC 4Fr Single Lumen Marked catheter, 70 cm guidewire - Basic Kit (70001302); HydroPICC 4Fr Single Lumen Marked catheter - Maximal Barrier kit (70001304); HydroPICC 5Fr Dual Lumen Marked catheter, 130 cm guidewire - Basic Kit (70002301); HydroPICC 5Fr Dual Lumen Marked catheter, 70 cm guidewire - Basic Kit (70002302); HydroPICC 5Fr Dual Lumen Marked catheter - Maximal Barrier kit (70002304); Hydr
Applicant
Access Vascular, Inc.
510(k) number
K243458
Product code
LJS
Decision
Substantially Equivalent (SESE)
Decision date
2025-08-01
Date received
2024-11-08
Regulation
880.5970
Classification name
Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Brian Hanley
Address
749 Middlesex Tpke. Ballerica MA US 01821 01821

FDA Registration Numbers

Source Documents

510(k) summary PDF

Other 510(k) Records For Product Code LJS

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