Surgitek
Surgitek holds FDA 510(k) medical device clearances, first cleared 1983, most recent 1995.
Top product codes for Surgitek
Recent clearances by Surgitek
- K946296 — QUADRA-COIL URETERAL STENT
- K944391 — OM-4 (TENATIVE) URODYNAMIC MEASRUEMENT SYSTEM
- K943491 — RIGHT ANGLE UROLOGIC LASER FIBER
- K941952 — SURGITEK INFUSER
- K933260 — HELICAL STONE/FLATWIRE STONE BASKETS
- K933261 — GRASPING FORCEPS
- K930733 — URETERAL STENT
- K930483 — URETERAL CATHETER
- K926344 — HYDROPHILIC COATED GUIDEWIRE
- K920451 — ENDOTEK ULTRA SYSTEM
- K922542 — GRASPING FORCEPS
- K904793 — SURGITEK GRADUATED URETEROSCOPE (MODEL GU-8)
- K904797 — SURGITEK GRADUATED CYSTOSCOPE (MODEL GC-16)
- K905015 — SURGITEK ERECTEK TM EXTERNAL ERECTION DEVICE
- K902349 — SURGITEK INTRA-SPAN INTRAOPERATIVE TISSUE EXPANDER
- K894495 — SURGITEK(R) EXTERNAL FILL PORT
- K891339 — IRRI-FLO IRRIGATION DELIVERY SYSTEM
- K880660 — SURGITEK SUPER DOUBLE J URETERAL STENT KIT
- K875333 — SURGITEK NPT MONITOR
- K872353 — SURGITEK INFUSION STENT SYSTEM*
- K870518 — SURGITEK PHYSICIAN DISPEN. PATIENT SELF-INJECT KIT
- K863492 — METAL TIPPED URETER. STENT & MAGNETIC STENT RETRI.
- K833782 — SURGITEK ALL SILICONE INFECTION DOUBJ
- K834347 — FLEXI-FLATE PENILE IMPLANT
- K840464 — TISSUE EXPANDER
- K840059 — SILITEK URINARY DIVERSION STENT
- K833297 — BRONCHOSCOPY TUBE W/ULTRA LOCUFF
- K833628 — LUMEN-4 URODYNAMIC CATHETER
- K832915 — URETHRAL OBSTRUCT PRIMARY EXCHANGE STEN
Data sourced from openFDA. This site is unofficial and independent of the FDA.