Hmg 1

• FDA 510(k) K172763 decided 4 Jun 2018 Active
• FDA GUDID UDI-DI 10850048235011 listed 25 Apr 2023 Listed

1. 4 Jun 2018 Cleared FDA 510(k) K172763
2. 25 Apr 2023 Listed FDA GUDID 10850048235011

Trade name

Hmg

Generic name

Blood collection set, noninvasive

Model / reference

1

Primary DI / UDI-DI

10850048235011

510(k) Number

K172763 ↗

FDA product code

JKA

GMDN term

Blood collection set, noninvasive

Device class

Class II

Regulation number

862.1675

GUDID distribution status

In Commercial Distribution

Category: Blood collection set, noninvasive

Other devices filed under FDA product code JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection).

• GREINER VACUETTE BLOOD COLLECTION TUBE by Greiner America, Inc.
• S-Monovette® 02.1063.100 by Sarstedt Aktiengesellschaft & Co.KG
• BD Vacutainer Serum Separator (SST) Blood Collection Tubes by Becton, Dickinson and Company
• SAFETEX COMBINATION BLOOD (ALCOHOL, ETHYL) / URINE COLLECTION AND TRANSPORT KIT by Andwin Scientific
• Navi™ Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG) by Venocare, Inc.
• SERI-SEP by Torval Corp.
• DORN BLOOD CULTURE COLLECTION TUBE by Wadley Institutes of Molecular Medici
• BD Vacutainer® UltraTouch™ Push Button 368686 by Becton, Dickinson and Company
• MINICOLLECT CAPILLARY BLOOD COLLECTION TUBES by GREINER BIO-ONE NORTH AMERICA, INC.
• Micro-Needle 85.923 by Sarstedt Aktiengesellschaft & Co.KG

• HMG Needleless PRN connector CV2

  Class II

  GUDID on market

• HMG Pump Driven IV Administration Set PCA1001

  Class II

  FDA 510(k) K150513 Active Cleared 28 May 2015 GUDID on market

• HMG Pump Driven IV Administration Set PCA1002

  Class II

  FDA 510(k) K150513 Active Cleared 28 May 2015 GUDID on market

• HMG IV extension sets- CIV007

  Class II

  FDA 510(k) K150513 Active Cleared 28 May 2015 GUDID on market

See all devices from Hartman Medical Group LLC →