Turbo-Ject Peripherally Inserted Central Venous Catheter (Picc)

FDA 510(k) K111244 · Cook, Inc.

Substantially Equivalent

510(k) numberK111244

Submission

Device name
Turbo-Ject Peripherally Inserted Central Venous Catheter (Picc)
Applicant
Cook, Inc.
Bloomington, IN, US
Received
May 3, 2011
Decision date
June 14, 2011
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LJS – Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5970
Specialty
General Hospital
Implant
Yes

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Questions and answers

When was Turbo-Ject Peripherally Inserted Central Venous Catheter (Picc) cleared by the FDA?

Turbo-Ject Peripherally Inserted Central Venous Catheter (Picc) (K111244) received a 510(k) decision of Substantially Equivalent on June 14, 2011, 42 days after the submission was received.

What is the product code of K111244?

The FDA product code is LJS – Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days, a Class II (moderate risk) device regulated under 21 CFR 880.5970.