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FDA 510(k)

VAS-CATH URETERAL STENTS CATHETER, MODIFICATION

K-Number: K905505 · 1991-04-09

ApplicantVas-Cath, Inc.
Decision Date1991-04-09
Product CodeFAD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VAS-CATH URETERAL STENTS CATHETER, MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Vas-Cath, Inc.. It received FDA 510(k) clearance on 1991-04-09 under 510(k) number K905505. 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 VAS-CATH URETERAL STENTS CATHETER, MODIFICATION?

VAS-CATH URETERAL STENTS CATHETER, MODIFICATION is a medical device that received FDA 510(k) clearance on 1991-04-09. The listed applicant is Vas-Cath, Inc.. The 510(k) number is K905505.

When did VAS-CATH URETERAL STENTS CATHETER, MODIFICATION receive FDA 510(k) clearance?

VAS-CATH URETERAL STENTS CATHETER, MODIFICATION received FDA 510(k) clearance on 1991-04-09, under 510(k) number K905505.

Who is the listed applicant for VAS-CATH URETERAL STENTS CATHETER, MODIFICATION?

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

What is the FDA product code for VAS-CATH URETERAL STENTS CATHETER, MODIFICATION?

The FDA product code for VAS-CATH URETERAL STENTS CATHETER, MODIFICATION is FAD.

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Other records listing Vas-Cath, 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.

K973013OPTI-PLAST (CENTURION) 5.5F ANGIOPLASTY CATHETERK965178NIAGARA DUAL LUMEN CATHETERK964881ULTRAVERSE PTA CATHETERK970725OPTI-PLAST XL 5.5 F PTA CATHETERK941706OPTI-PLAST ANGIOPLASTY CATHETERK925485VAS-CATH INC. OPTI-PLAST ANGIOPLASTY CATHETER

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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

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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