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FDA 510(k)

URETEROMAT 4400

K-Number: K915751 · 1992-04-24

ApplicantF.M. Wiest USA, Inc.
Decision Date1992-04-24
Product CodeEZN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

URETEROMAT 4400 is the device name listed in this FDA 510(k) record. The listed applicant is F.M. Wiest USA, Inc.. It received FDA 510(k) clearance on 1992-04-24 under 510(k) number K915751. The device is classified under product code EZN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URETEROMAT 4400?

URETEROMAT 4400 is a medical device that received FDA 510(k) clearance on 1992-04-24. The listed applicant is F.M. Wiest USA, Inc.. The 510(k) number is K915751.

When did URETEROMAT 4400 receive FDA 510(k) clearance?

URETEROMAT 4400 received FDA 510(k) clearance on 1992-04-24, under 510(k) number K915751.

Who is the listed applicant for URETEROMAT 4400?

The FDA 510(k) record lists F.M. Wiest USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for URETEROMAT 4400?

The FDA product code for URETEROMAT 4400 is EZN.

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Other records listing F.M. Wiest USA, Inc. as applicant

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Related Devices (Code: EZN)

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.

K250910Optilume® High Pressure Urological Balloon Dilation CatheterUrotronic, Inc.K220781ARMADA Ureteral Dilator Set, ARMADA Nottingham One Step Dilator, ARMADA Amplatz Renal Dilator Sets, ARMADA Renal Dilator, Glider Amplatz Sheath, ARMADA Renal Dilator with Amplatz Sheath, Fascial Dilator Set, Introducer Sheath, Introducer CatheterAllwin Medical Devices, Inc.K201007In-Ka Ureteral Balloon Dilatation CatheterColoplast Corp.K190612EQUINOX Balloon Dilatation CatheterDornier Medtech America, Inc.K173654Ureteral Dilator Sets, Ureteral DilatorsCook IncorporatedK180756Safety Wire Guide IntroducerCook Incorporated

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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