Delflex Rigid Drain Container

No FDA recalls on record, checked 10 Oct 2026.

510(k) Number

K871155 ↗

FDA Product Code

KDJ

Device Class

Class II

Regulation

21 CFR Part 876.5630

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

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• Intertech Sterile Water for Inhalation

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  FDA 510(k) K881184 Active Cleared 25 May 1988

• Delmed 80/2 Dialysis System W/Last Bag Option

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  FDA 510(k) K901478 Active Cleared 27 Jul 1990

• Empty Transfer Bag

  Class II

  FDA 510(k) K791673 Active Cleared 23 Oct 1979

• Albumin Intravenous Administration Set

  Class II

  FDA 510(k) K791672 Active Cleared 26 Oct 1979

• Hospal Dialysate for C.A.V.H.D.

  Class II

  FDA 510(k) K872857 Active Cleared 5 Oct 1987

See all devices from Delmed, Inc. →