First PICC™

FDA UDI

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name: First PICC™ FDA UDI
Generic Name: Peripherally-inserted central venous catheter FDA UDI
Device Name: First PICC™ S/L Peripherally Inserted Central Catheter 26ga (1.9F) 0.65mm x 50cm with Statlock® Stabilization Device FDA UDI
Model / Reference: 384242 FDA UDI
Description: First PICC™ S/L Peripherally Inserted Central Catheter 26ga (1.9F) 0.65mm x 50cm with Statlock® Stabilization Device FDA UDI

Identifiers

Catalog Number: 384242 FDA UDI
Primary DI / UDI-DI: 00886333209774 FDA UDI
510(k) Number: K972262 FDA UDI
FDA Product Code: FOZ FDA UDI
GMDN Term: Peripherally-inserted central venous catheter FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Peripherally-inserted central venous catheter

First PICC™ by Argon Medical Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripherally-inserted central venous catheter.

BioFlo — NAVILYST MEDICAL, INC. · Class II
Synergy — Health Line International Corp · Class II
ARROW — TELEFLEX INCORPORATED · Class II
ARROW — TELEFLEX INCORPORATED · Class II
PowerPICC — Bard Access Systems, Inc. · Class II
ARROW — TELEFLEX INCORPORATED · Class II
PowerPICC Provena — Bard Access Systems, Inc. · Class II
BioFlo — NAVILYST MEDICAL, INC. · Class II

Cleared under the same submission

K972262 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Argon Medical Devices, Inc.

Sources (1)

FDA UDI 5e20184d-1551-484f-bd31-ce80378e2118 38 fields · synced Jun 9, 2026