Micro-6-Series (Mr-6, Mr-6l) Ureteroscopes, Mro-6 Series (Mr-633, Mr-642) Ureteroscopes, Mro-7 Series (Mro-733) Ureteros

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K011849 ↗

FDA Product Code

FGB

Device Class

Class II

Regulation

21 CFR Part 876.1500

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Circon Aeh-4 Electrohydraulic Lithotripsy Probe

  Class II

  FDA 510(k) K011848 Active Cleared 11 Sep 2001

• Circon Acmi Hydrolaparoscope(Tm) Instrument

  Class II

  FDA 510(k) K911053 Active Cleared 3 Jun 1991

• Circon Endotek Om-4 H2O Cystometry Pump

  Class II

  FDA 510(k) K970595 Active Cleared 24 Oct 1997

• Ureteroscope, Pediatric Cystoureteroscope, Operating Pediatric Cystoureteroscope, Models Mr-9, Mr-9l,

  Class II

  FDA 510(k) K012758 Active Cleared 9 Apr 2002

• Circon Acmi Gen Surg Instru for Mini Invasive Surg

  Class II

  FDA 510(k) K914883 Active Cleared 15 Jan 1993

• Apn-2 USA Series Flexible Choledochoscope

  Class II

  FDA 510(k) K012951 Active Cleared 9 Nov 2001

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