Jelco 96002

• FDA 510(k) K923090 decided 1 Sep 1992 Active
• FDA GUDID UDI-DI 20351688062960 listed 9 Jan 2017 Listed

1. 1 Sep 1992 Cleared FDA 510(k) K923090
2. 9 Jan 2017 Listed FDA GUDID 20351688062960

Trade name

Jelco

Generic name

Blood collection tube holder, single-use

Model / reference

96002

Primary DI / UDI-DI

20351688062960

510(k) Number

K923090 ↗

FDA product code

JKA

GMDN term

Blood collection tube holder, single-use

Device class

Class II

Regulation number

862.1675

GUDID distribution status

In Commercial Distribution

Category: Blood collection tube holder, single-use

Other devices filed under FDA product code JKA (Tubes, vials, systems, serum separators, blood collection).

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• CellSave 952820 by Menarini Silicon Biosystems Inc.
• BD Vacutainer® UltraTouch™ Push Button Blood Collection Set with PAH 368684 by Becton, Dickinson and Company
• safePICO70 956-608 by Radiometer Medical ApS
• BD Vacutainer® Luer-Lok™ Access Device 36490200 by Becton, Dickinson and Company
• S-Monovette® 04.1935.001 by Sarstedt Aktiengesellschaft & Co.KG
• Monarch Blood Collection Set by The Monarch Company
• 20G Open-System Ally Device Kit (AV100000), 22G Open-System Ally Device Kit (AV110000) by Avia Vascular
• BLOOD CULTURE HOLDER by GREINER BIO-ONE NORTH AMERICA, INC.
• PICO70 956-529 by Radiometer Medical ApS

• Bivona FT26JN30NGF219N

  Class II

  FDA 510(k) K923878 Active Cleared 29 Dec 1992 GUDID on market

• Bivona HT26JS70NSC222N

  Class II

  FDA 510(k) K923878 Active Cleared 29 Dec 1992 GUDID on market

• Bivona HT26JS80NSC205N

  Class II

  FDA 510(k) K923878 Active Cleared 29 Dec 1992 GUDID on market

• Bivona ST26JN55NSA204N

  Class II

  FDA 510(k) K923878 Active Cleared 29 Dec 1992 GUDID on market

See all devices from ICU Medical, Inc. →