Rivetti-Levinson Instraluminal Shunt

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K972261 ↗

FDA Product Code

DWF

Device Class

Class II

Regulation

21 CFR Part 870.4210

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Peritoneal/Cardiac Catheter

  Class II

  FDA 510(k) K970983 Active Cleared 13 Jun 1997

• Neuroview Instrument Holder, Model 300-33

  Class II

  FDA 510(k) K992006 Active Cleared 17 Aug 1999

• Beverly Referential Valve (NL850-9710) with Integral Peritoneal Catheter (NL850-9720) Valve Kit (NL850-9730)

  Class II

  FDA 510(k) K981246 Active Cleared 26 May 1999

• Novus Standard and Pediatric Valves

  Class II

  FDA 510(k) K961859 Active Cleared 16 Dec 1996

• Shunt Tap with Icp Monitoring Access Port

  Class II

  FDA 510(k) K964371 Active Cleared 31 Jan 1997

• Maurice Worldwide Shunt System

  Class II

  FDA 510(k) K973525 Active Cleared 16 Dec 1997

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