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510(k) K913928

SURGITEK(R) 4.5FR LUBRI-FLEX(TM) URETERAL STENT by Surgitek Medical Engineering Corp. — Product Code FAD

K913928 is an FDA 510(k) premarket notification submitted by Surgitek Medical Engineering Corp. for the device "SURGITEK(R) 4.5FR LUBRI-FLEX(TM) URETERAL STENT". The FDA issued a decision of Substantially Equivalent on November 19, 1991. The device falls under product code FAD (Stent, Ureteral), a Class II device regulated under 21 CFR 876.4620. Surgitek Medical Engineering Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 19, 1991
Date Received
September 3, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stent, Ureteral
Device Class
Class II
Regulation Number
876.4620
Review Panel
GU
Submission Type

Other clearances by Surgitek Medical Engineering Corp.

  • K914504 — CYTOLOGY BRUSH (February 18, 1992)
  • K914495 — E.R.C.P. CATHETER (January 30, 1992)
  • K914497 — BIOPSY FORCEPS (January 3, 1992)
  • K914505 — STONE BASKET (December 9, 1991)
  • K914496 — SCLEROTHERAPY NEEDLE (December 5, 1991)
  • K914503 — GRASPING FORCEPS (December 5, 1991)
  • K913294 — SURGITEK(R) LAPAROSCOPIC CHOLANGIOGRAM KIT (October 4, 1991)
  • K910769 — SURGITEK(R) ERCP CONTRAST MEDIA SYSTEM (June 25, 1991)
  • K910768 — SURGITEK(R) 420 CM G.I. INFUSION GUIDEWIRE (March 19, 1991)
  • K903127 — SURGITEK(R) TURP MONITOR (October 9, 1990)

Other clearances for product code FAD

  • K251890 — Disposable Ureteral Stents (February 20, 2026)
  • K251469 — Endura™ Ureteral Stent and Stent Set (December 19, 2025)
  • K243039 — Ureteral Stents (AF-D series) (June 18, 2025)
  • K243830 — Disposable ureteral stent (May 14, 2025)
  • K250824 — Percuflex Ureteral Stent; Percuflex Plus Ureteral Stent; Percuflex Plus SureDriv (April 15, 2025)
  • K232920 — RELIEF™ Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF™ Ureteral Stent (March 22, 2024)
  • K211934 — APDL Drainage Catheter System, Flexima APDL Drainage Catheter System, Flexima AP (November 10, 2022)
  • K213185 — ImaJin Silicone double loop ureteral stent kits, ImaJin Pyelostent Silicone doub (June 8, 2022)
  • K213444 — RELIEF Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF Ureteral Stent Ki (March 17, 2022)
  • K213186 — NovoFlow Reinforced Ureteral Stent (February 16, 2022)

FDA data resources