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FDA 510(k)

Medline Epidural Catheter

K-Number: K150731 · 2016-03-07

ApplicantMedline Industries, Inc.
Decision Date2016-03-07
Product CodeBSO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Medline Epidural Catheter is a medical device manufactured by Medline Industries, Inc.. It received FDA 510(k) clearance on 2016-03-07 under approval number K150731. The device is classified under product code BSO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medline Epidural Catheter?

Medline Epidural Catheter is a medical device that received FDA 510(k) clearance on 2016-03-07. It is manufactured by Medline Industries, Inc.. The 510(k) number is K150731.

When was Medline Epidural Catheter approved by the FDA?

Medline Epidural Catheter received FDA 510(k) clearance on 2016-03-07, under approval number K150731.

What company makes Medline Epidural Catheter?

Medline Epidural Catheter is manufactured by Medline Industries, Inc..

What is the FDA product code for Medline Epidural Catheter?

The FDA product code for Medline Epidural Catheter is BSO.

Related Clinical Trials

NCT05606952 Color Doppler to Confirm Epidural Catheter Positioning in Parturient COMPLETED NCT06556836 "Diagnostic Accuracy of Ultrasound Compared to Epidurography for Epidural Catheter Localization" COMPLETED

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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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