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FDA 510(k)

STORZ MODULITH, MODEL SLX-F2

K-Number: K040476 · 2004-08-26

ApplicantKARL STORZ Endoscopy-America, Inc.
Decision Date2004-08-26
Product CodeLNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STORZ MODULITH, MODEL SLX-F2 is the device name listed in this FDA 510(k) record. The listed applicant is KARL STORZ Endoscopy-America, Inc.. It received FDA 510(k) clearance on 2004-08-26 under 510(k) number K040476. 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 STORZ MODULITH, MODEL SLX-F2?

STORZ MODULITH, MODEL SLX-F2 is a medical device that received FDA 510(k) clearance on 2004-08-26. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K040476.

When did STORZ MODULITH, MODEL SLX-F2 receive FDA 510(k) clearance?

STORZ MODULITH, MODEL SLX-F2 received FDA 510(k) clearance on 2004-08-26, under 510(k) number K040476.

Who is the listed applicant for STORZ MODULITH, MODEL SLX-F2?

The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STORZ MODULITH, MODEL SLX-F2?

The FDA product code for STORZ MODULITH, MODEL SLX-F2 is LNS.

Related Clinical Trials

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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Other records listing KARL STORZ Endoscopy-America, Inc. 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.

K252624KARL STORZ Laryngoscopes and AccessoriesK240506KARL STORZ HoldersK223885HOPKINS TelescopesK230359KOH Ultramicro Injection Cannula (26167NN); Suction a. Irrig. Cannula,L. 36cm (37360CP); Suction a. Irrig. Cannula,L. 36cm (37360SC); Suction and Irrig Cannula,l. 36cm (37560LH); Suction a. Irrig. Cannula,L. 30cm (37260LH); KOH Ultramicro Injection Needle (26167NA); Puncture Needle, LUER-lock (26178R); Suction a. Irrig. Cannula,L. 43cm (37460LH); Suction a. Irrig. Cannula,L. 36cm (37360LH); Puncture Needle, dia. 1.6 mm, 36 cm (26175R); Two-Way Stopcock (26167H); Injection Needle, LUER-K223520UNIDRIVE SIII SystemK223923HOPKINS Telescopes

View all 355 devices →

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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