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FDA 510(k)

UROPOWER

K-Number: K022721 · 2003-08-26

ApplicantW.O.M. World of Medicine AG
Decision Date2003-08-26
Product CodeEXY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

UROPOWER is the device name listed in this FDA 510(k) record. The listed applicant is W.O.M. World of Medicine AG. It received FDA 510(k) clearance on 2003-08-26 under 510(k) number K022721. The device is classified under product code EXY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UROPOWER?

UROPOWER is a medical device that received FDA 510(k) clearance on 2003-08-26. The listed applicant is W.O.M. World of Medicine AG. The 510(k) number is K022721.

When did UROPOWER receive FDA 510(k) clearance?

UROPOWER received FDA 510(k) clearance on 2003-08-26, under 510(k) number K022721.

Who is the listed applicant for UROPOWER?

The FDA 510(k) record lists W.O.M. World of Medicine AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UROPOWER?

The FDA product code for UROPOWER is EXY.

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Other records listing W.O.M. World of Medicine AG as applicant

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Related Devices (Code: EXY)

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.

K971913GR100F URINE FLOWMETERAlbyn Medical , Ltd.K953999DANTEC DA CAPODantec Medical, Inc.K951442FLOLABSynectics Medical, Inc.K944972URO-GRAM CYSTOMRTROGRAM WITH UROFLOWMETRYMyo/Kinetic Systems, Inc.K9454954-CHANNEL URODYNAMIC MONITOR WITH URO-FLO OPTIONFiberoptic Sensor Technlogies, Inc.K941105UORCAP,MODEL NUMBER UDS-UCAPLaborie Medical Tech, Inc.

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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