Tube, Feeding, Argyle

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

510(k) Number

K760137 ↗

FDA Product Code

FPD

Device Class

Class II

Regulation

21 CFR Part 876.5980

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Lancer Glucose Rate Reagent Kit

  Class II

  FDA 510(k) K801071 Active Cleared 23 May 1980

• Blood Collection Tube, Lavender

  Class II

  FDA 510(k) K771052 Active Cleared 27 Jun 1977

• Catheter, Argyle Thoracic

  Class I

  FDA 510(k) K760351 Active Cleared 23 Aug 1976

• Sump Drain, W/Filter, Argyle Edlich

  Class I

  FDA 510(k) K770442 Active Cleared 30 Mar 1977

• Lancer L-Ina Human Reference Serum

  Class II

  FDA 510(k) K792013 Active Cleared 13 Nov 1979

• Reagent Kit, Lancer Glucose

  Class I

  FDA 510(k) K790197 Active Cleared 12 Mar 1979

See all devices from Sherwood Medical Industries →