Dobbhoff(R) Retrieval Forceps

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

510(k) Number

K901744 ↗

FDA Product Code

KQW

Device Class

Class I

Regulation

21 CFR Part 888.1520

Advisory Committee

Orthopedic

FDA Decision

SESE Substantially Equivalent

• Entron Enteral Feeding Bag

  Class II

  FDA 510(k) K850134 Active Cleared 14 Feb 1985

• Peewee Replacement Gastrostomy Tube

  Class II

  FDA 510(k) K903662 Active Cleared 12 Dec 1990

• Islami Gastrointestinal Tube

  Class II

  FDA 510(k) K834268 Active Cleared 4 Feb 1984

• Pedi-Tube Pediatric Feeding Tube

  Class II

  FDA 510(k) K822875 Active Cleared 13 Oct 1982

• Enteral Feeding Tube

  Class II

  FDA 510(k) K051480 Active Cleared 12 Oct 2005

• Ambi-24 Ph/Pressure Monitor

  Class I

  FDA 510(k) K854514 Active Cleared 24 Feb 1986

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