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FDA 510(k)

TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER (PICC)

K-Number: K111244 · 2011-06-14

ApplicantCook, Inc.
Decision Date2011-06-14
Product CodeLJS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER (PICC) is the device name listed in this FDA 510(k) record. The listed applicant is Cook, Inc.. It received FDA 510(k) clearance on 2011-06-14 under 510(k) number K111244. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER (PICC)?

TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER (PICC) is a medical device that received FDA 510(k) clearance on 2011-06-14. The listed applicant is Cook, Inc.. The 510(k) number is K111244.

When did TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER (PICC) receive FDA 510(k) clearance?

TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER (PICC) received FDA 510(k) clearance on 2011-06-14, under 510(k) number K111244.

Who is the listed applicant for TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER (PICC)?

The FDA 510(k) record lists Cook, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER (PICC)?

The FDA product code for TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER (PICC) is LJS.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Cook, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K133634SPECTRUM TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER SETK132020ADVANCE 34LP LOW PROFILE PTA BALLOON DILATATION CATHETERK131201ENTUIT SECURE GASTROINTESTIONAL SUTURE ANCHOR SET, ENTUIT SECURE ADJUSTABLE GASTROINTESTINAL SUTURE ANCHOR SETK131206COOK CERVICAL RIPENING BALLOONK132334TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER (PICC) SETK122091COOK TURBO-FLO HD ACUTE HEMODIALYSIS CATHETER SET/TRAY COOK SPECTRUM TURBO-FLO HD ACUTE HEMODIALYSIS CATHETER SET/TRAY

View all 184 devices →

Related Devices (Code: LJS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260929Neonav ECG Tip Location SystemNavi Medical TechnologiesK252373BioFlo Hybrid PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology; BioFlo Midline Catheter; Xcela Power Injectable PICC; Xcela PICC with PASV Valve Technology; Xcela Hybrid PICC with PASV Valve TechnologySpectrum VascularK252792PM2™ System with ECGuide™ ConnectorPiccolo Medical, Inc.K243458HydroPICC 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); HydrAccess Vascular, Inc.K251212Dual Lumen 5Fr HydroPICC Catheter (PICC-251CM) (PICC-251CM); Dual Lumen 5Fr HydroPICC Catheter (PICC-252CM) (PICC-252CM)Access Vascular, Inc.K243484PM2+ System and SmartPICC StyletPiccolo Medical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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