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FDA 510(k)

ECONOLITH E3000, MODEL 3000 (SW-6)

K-Number: K040461 · 2004-05-25

ApplicantMedispec, Ltd.
Decision Date2004-05-25
Product CodeLNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ECONOLITH E3000, MODEL 3000 (SW-6) is the device name listed in this FDA 510(k) record. The listed applicant is Medispec, Ltd.. It received FDA 510(k) clearance on 2004-05-25 under 510(k) number K040461. The device is classified under product code LNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECONOLITH E3000, MODEL 3000 (SW-6)?

ECONOLITH E3000, MODEL 3000 (SW-6) is a medical device that received FDA 510(k) clearance on 2004-05-25. The listed applicant is Medispec, Ltd.. The 510(k) number is K040461.

When did ECONOLITH E3000, MODEL 3000 (SW-6) receive FDA 510(k) clearance?

ECONOLITH E3000, MODEL 3000 (SW-6) received FDA 510(k) clearance on 2004-05-25, under 510(k) number K040461.

Who is the listed applicant for ECONOLITH E3000, MODEL 3000 (SW-6)?

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

What is the FDA product code for ECONOLITH E3000, MODEL 3000 (SW-6)?

The FDA product code for ECONOLITH E3000, MODEL 3000 (SW-6) is LNS.

Related Clinical Trials

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Other records listing Medispec, Ltd. 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.

K210166Omnispec ED1000K063504ECONOLITH EM1000K974796LITHOSPEC(TM) INTRACORPOREAL LITHOTRIPTER

Related Devices (Code: LNS)

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.

K261086Break WaveSonomotion, Inc.K252913Break WaveSonomotion, Inc.K242922Extracorporeal Shock Wave Lithotripter (U200)Shenzhen Wikkon Precision Technologies Co., Ltd.K221903Delta III ProDornier Medtech America, Inc.K213772LM-9300 Plus LithotripterLite-Med, Inc.K201001Modulith SLX-F2Karl Storz Endoscopy America

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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