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FDA 510(k)

MEMCATH UROLOGY CATHETER, MODEL 101 -000 - 006

K-Number: K993226 · 1999-12-10

ApplicantMemcath Technologies, LLC
Decision Date1999-12-10
Product CodeEZD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEMCATH UROLOGY CATHETER, MODEL 101 -000 - 006 is the device name listed in this FDA 510(k) record. The listed applicant is Memcath Technologies, LLC. It received FDA 510(k) clearance on 1999-12-10 under 510(k) number K993226. The device is classified under product code EZD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEMCATH UROLOGY CATHETER, MODEL 101 -000 - 006?

MEMCATH UROLOGY CATHETER, MODEL 101 -000 - 006 is a medical device that received FDA 510(k) clearance on 1999-12-10. The listed applicant is Memcath Technologies, LLC. The 510(k) number is K993226.

When did MEMCATH UROLOGY CATHETER, MODEL 101 -000 - 006 receive FDA 510(k) clearance?

MEMCATH UROLOGY CATHETER, MODEL 101 -000 - 006 received FDA 510(k) clearance on 1999-12-10, under 510(k) number K993226.

Who is the listed applicant for MEMCATH UROLOGY CATHETER, MODEL 101 -000 - 006?

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

What is the FDA product code for MEMCATH UROLOGY CATHETER, MODEL 101 -000 - 006?

The FDA product code for MEMCATH UROLOGY CATHETER, MODEL 101 -000 - 006 is EZD.

Related Clinical Trials

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Other records listing Memcath Technologies, LLC 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.

K000767MEMCATH UROLOGY INTRODUCER SHEATH, MODEL 201

Related Devices (Code: EZD)

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.

K261418Liquick X-treme, Liquick X-treme PlusTeleflex MedicalK260737Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Female (CH06 - CH16); Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Male Straight (CH06 - CH18); Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Male Coude (CH10 - CH18).ConvatecK261658LoFric Origo Pro CoudéWellspect ABK262045Luja SoftColoplast A.S.K260394Hydrophilic coated intermittent nalaton catheter for single use-ready to use (NCR)Hangzhou Jimushi Meditech Co., Ltd.K253295Coude Sleeved IC; Coude Plus Sleeved ICHollister Incorporated

Official Source

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

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