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Vortek Ureteral Double Loop Stent, Biosoft Ureteral Double Loop Stent

by International Regulatory Consultants 510(k)

Active United States

510(k) K981591

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Special NumberK981591 Date9 Oct 1998ClearedStatusActive

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
FAD
Device Class
Class II
Regulation
21 CFR Part 876.4620
Advisory Committee
Gastroenterology, Urology
FDA Decision
SESE Substantially Equivalent

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