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FDA 510(k)

Percutaneous Neonatal Pigtail Nephrostomy Set, Pediatric Nephrostomy Stent Set

K-Number: K181735 · 2019-03-27

ApplicantCook Incorporated
Decision Date2019-03-27
Product CodeLJE
DecisionUnknown

Device Summary

Percutaneous Neonatal Pigtail Nephrostomy Set, Pediatric Nephrostomy Stent Set is a medical device manufactured by Cook Incorporated. It received FDA 510(k) clearance on 2019-03-27 under approval number K181735. The device is classified under product code LJE. FDA Decision: Unknown.

Frequently Asked Questions

What is the Percutaneous Neonatal Pigtail Nephrostomy Set, Pediatric Nephrostomy Stent Set?

Percutaneous Neonatal Pigtail Nephrostomy Set, Pediatric Nephrostomy Stent Set is a medical device that received FDA 510(k) clearance on 2019-03-27. It is manufactured by Cook Incorporated. The 510(k) number is K181735.

When was Percutaneous Neonatal Pigtail Nephrostomy Set, Pediatric Nephrostomy Stent Set approved by the FDA?

Percutaneous Neonatal Pigtail Nephrostomy Set, Pediatric Nephrostomy Stent Set received FDA 510(k) clearance on 2019-03-27, under approval number K181735.

What company makes Percutaneous Neonatal Pigtail Nephrostomy Set, Pediatric Nephrostomy Stent Set?

Percutaneous Neonatal Pigtail Nephrostomy Set, Pediatric Nephrostomy Stent Set is manufactured by Cook Incorporated.

What is the FDA product code for Percutaneous Neonatal Pigtail Nephrostomy Set, Pediatric Nephrostomy Stent Set?

The FDA product code for Percutaneous Neonatal Pigtail Nephrostomy Set, Pediatric Nephrostomy Stent Set is LJE.

Related Clinical Trials

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Related Devices (Code: LJE)

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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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