Low Profile Gastrostomy

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

510(k) Number

K872771 ↗

FDA Product Code

KNT

Device Class

Class II

Regulation

21 CFR Part 876.5980

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Specimen Trap

  Class II

  FDA 510(k) K834467 Active Cleared 17 Feb 1984

• Jejunal Feeding Tube

  Class II

  FDA 510(k) K861309 Active Cleared 16 Dec 1986

• Replacement Gastrostomy Tube

  Class II

  FDA 510(k) K861323 Active Cleared 16 Dec 1986

• Papillotome

  Class II

  FDA 510(k) K851652 Active Cleared 24 Jun 1985

• Needle W/Stylet for Implantation

  Class I

  FDA 510(k) K854238 Active Cleared 13 Nov 1985

• Inflator/Deflator Piston Syringe

  Class II

  FDA 510(k) K860589 Active Cleared 7 Apr 1986

See all devices from Microvasive →