Lifeglobal Human Serum Albumin Lg Hsa

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K083509 ↗

FDA Product Code

MQL

FDA applicant

Genx Intl., Inc.

Device Class

Class II

Regulation

21 CFR Part 884.6180

Advisory Committee

Obstetrics/Gynecology

FDA Decision

SESE Substantially Equivalent

• <genx> Single Lumen Sideport Needle

  Class II

  FDA 510(k) K991264 Active Cleared 9 Sep 1999

• Genxcatheter

  Class II

  FDA 510(k) K963031 Active Cleared 21 Oct 1996

• Global by <genx> Blastocyst Media

  Class II

  FDA 510(k) K010183 Active Cleared 2 May 2001

• Allgrad Wash (Herpes Buffered Washing Medium)

  Class II

  FDA 510(k) K023033 Active Cleared 26 Nov 2002

• Htf Plus - Htf with Non-Essential Amino Acids

  Class II

  FDA 510(k) K022334 Active Cleared 28 Aug 2002

• Genx Microtools

  Class II

  FDA 510(k) K993884 Active Cleared 14 Feb 2000

See all devices from <Genx> Intl., Inc. →