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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 the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2016-03-07 under 510(k) 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. The listed applicant is Medline Industries, Inc.. The 510(k) number is K150731.

When did Medline Epidural Catheter receive FDA 510(k) clearance?

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

Who is the listed applicant for Medline Epidural Catheter?

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

What is the FDA product code for Medline Epidural Catheter?

The FDA product code for Medline Epidural Catheter is BSO.

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Related Devices (Code: BSO)

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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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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