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FDA 510(k)

MVM 7.5 FRENCH FLEXIBLE URETEROSCOPE

K-Number: K982905 · 1998-10-05

ApplicantKarl Storz Endoscopy
Decision Date1998-10-05
Product CodeFGB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MVM 7.5 FRENCH FLEXIBLE URETEROSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Karl Storz Endoscopy. It received FDA 510(k) clearance on 1998-10-05 under 510(k) number K982905. The device is classified under product code FGB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MVM 7.5 FRENCH FLEXIBLE URETEROSCOPE?

MVM 7.5 FRENCH FLEXIBLE URETEROSCOPE is a medical device that received FDA 510(k) clearance on 1998-10-05. The listed applicant is Karl Storz Endoscopy. The 510(k) number is K982905.

When did MVM 7.5 FRENCH FLEXIBLE URETEROSCOPE receive FDA 510(k) clearance?

MVM 7.5 FRENCH FLEXIBLE URETEROSCOPE received FDA 510(k) clearance on 1998-10-05, under 510(k) number K982905.

Who is the listed applicant for MVM 7.5 FRENCH FLEXIBLE URETEROSCOPE?

The FDA 510(k) record lists Karl Storz Endoscopy as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MVM 7.5 FRENCH FLEXIBLE URETEROSCOPE?

The FDA product code for MVM 7.5 FRENCH FLEXIBLE URETEROSCOPE is FGB.

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Other records listing Karl Storz Endoscopy as applicant

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Related Devices (Code: FGB)

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.

K261447CVAC® Aspiration SystemCalyxo, Inc.K262488Single-Use Video Flexible Ureterorenoscope (RP-U-C06R9, RP-U-C06R3, RP-U-C06S9, RP-U-C06S3)Guangzhou Red Pine Medical Instrument Co., Ltd.K261153LithoVue Elite Digital Flexible Ureteroscope SystemBoston Scientific CorporationK262552Single-use Flexible Ureteroscope (Single-use Flexible Ureteroscope: SUV-5C-B)Scivita Medical Technology Co., Ltd.K253505Zamenix™ PRoen Surgical, Inc.K260516BubbleView Single-Use Digital Flexible Cystoscope (C38-CS, C38-CRS, C50-C, C50-CR, C50-CB, C50-CBR)MacroLux Medical Technology Co., Ltd.

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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