Stent, Ureteral
FDA product code FAD · 121 cleared devices
Class 2
Gastroenterology, Urology
- Regulation
- 21 CFR 876.4620
- Review panel
- GU
- Implant
- Yes
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1978-12-07 – 2026-02-20
FAD
1986-09-09
FAD
1986-05-15
BARD DOUBLE PIGTAIL URETERAL STENT
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FAD
1986-04-03
MARDIS DANGLER URETERAL STENT SET
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FAD
1986-03-14
UROFLEX
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FAD
1986-03-11
MENTOR SINGLE COIL URINARY DIVERSION STENT SET
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FAD
1986-02-10
CURITY URETERAL STENT
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FAD
1985-09-05
URETERAL STENT
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FAD
1985-07-02
MENTOR UNIVERSAL URETERAL STENT SET
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FAD
1985-03-07
MENTOR DBL-COIL INDWELL. SILICONE URETERAL STENT S
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FAD
1985-02-28
MENTOR DBL-COIL INDWELLING POLYURETHANE URETERAL-
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FAD
1984-04-02
SURGITEK ALL SILICONE INFECTION DOUBJ
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FAD
1984-03-22
URETERAL DOUBLE PIGTAIL STENT
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FAD
1984-02-04
SILITEK URINARY DIVERSION STENT
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FAD
1983-10-14
URETHRAL OBSTRUCT PRIMARY EXCHANGE STEN
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FAD
1983-08-11
SURGITEK PERCUTANEOUS ARNEGRADE SILITEK
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FAD
1983-06-22
SURGITEK NEPHROSTENT KIT
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FAD
1983-05-27
BARD URETERAL STENT
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FAD
1983-05-09
SURGITEKS PERCUTANEOUS ANTEGRADE ALL -
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FAD
1982-04-26
URETERAL STANT SET
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FAD
1980-02-26
SURGITEK URINARY DIVERSION STENT
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FAD
1978-12-07
SURGITEK DOUBLE J URETEROL STENT
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