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FDA 510(k)

MEDLINE LATEX FOLEY CATHETER

K-Number: K071423 · 2007-07-18

ApplicantMedline Industries, Inc.
Decision Date2007-07-18
Product CodeEZL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDLINE LATEX FOLEY 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 2007-07-18 under 510(k) number K071423. The device is classified under product code EZL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDLINE LATEX FOLEY CATHETER?

MEDLINE LATEX FOLEY CATHETER is a medical device that received FDA 510(k) clearance on 2007-07-18. The listed applicant is Medline Industries, Inc.. The 510(k) number is K071423.

When did MEDLINE LATEX FOLEY CATHETER receive FDA 510(k) clearance?

MEDLINE LATEX FOLEY CATHETER received FDA 510(k) clearance on 2007-07-18, under 510(k) number K071423.

Who is the listed applicant for MEDLINE LATEX FOLEY 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 LATEX FOLEY CATHETER?

The FDA product code for MEDLINE LATEX FOLEY CATHETER is EZL.

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Related Devices (Code: EZL)

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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