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FDA 510(k)

FOSSA URETERAL OPEN STENTS

K-Number: K072293 · 2008-08-06

ApplicantFossa Medical, Inc.
Decision Date2008-08-06
Product CodeFAD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FOSSA URETERAL OPEN STENTS is the device name listed in this FDA 510(k) record. The listed applicant is Fossa Medical, Inc.. It received FDA 510(k) clearance on 2008-08-06 under 510(k) number K072293. The device is classified under product code FAD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOSSA URETERAL OPEN STENTS?

FOSSA URETERAL OPEN STENTS is a medical device that received FDA 510(k) clearance on 2008-08-06. The listed applicant is Fossa Medical, Inc.. The 510(k) number is K072293.

When did FOSSA URETERAL OPEN STENTS receive FDA 510(k) clearance?

FOSSA URETERAL OPEN STENTS received FDA 510(k) clearance on 2008-08-06, under 510(k) number K072293.

Who is the listed applicant for FOSSA URETERAL OPEN STENTS?

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

What is the FDA product code for FOSSA URETERAL OPEN STENTS?

The FDA product code for FOSSA URETERAL OPEN STENTS is FAD.

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 Fossa Medical, 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.

K033368FOSSA URETERAL OPEN LUMEN STENTK031292MODIFICATION TO FOSSA URETERAL STONE SWEEPER

Related Devices (Code: FAD)

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.

K251890Disposable Ureteral StentsZhejiang Chuangxiang Medical Technology Co., Ltd.K251469Endura™ Ureteral Stent and Stent SetCathegenix (Xiamen) Co., Ltd.K243039Ureteral Stents (AF-D series)Alton (Shanghai) Medical Instruments Co., Ltd.K243830Disposable ureteral stentShenzhen Trious Medical Technology Co., Ltd.K250824Percuflex Ureteral Stent; Percuflex Plus Ureteral Stent; Percuflex Plus SureDrive Steerable Ureteral Stent Set; Contour Ureteral Stent; Contour SureDrive Steerable Ureteral Stent Set; Contour VL Variable Length Ureteral Stent; Contour VL SureDrive Steerable Ureteral Stent Set; Polaris Ultra Ureteral Stent; Polaris Loop Ureteral Stent; Tria Firm Ureteral Stent; Tria Soft Ureteral Stent; Percuflex Urinary Diversion Stent SetBoston Scientific CorporationK232920RELIEF™ Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF™ Ureteral Stent Kit; Model: RS-002 - 6 Fr x 26cmUreteral Stent Company

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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