The following data is part of a premarket notification filed by Ganz Industries Sdn. Bhd. with the FDA for Acrylic Dipped Latex Examination Gloves - Sterile.
Device ID | K945504 |
510k Number | K945504 |
Device Name: | ACRYLIC DIPPED LATEX EXAMINATION GLOVES - STERILE |
Classification | Latex Patient Examination Glove |
Applicant | GANZ INDUSTRIES SDN. BHD. PT NO. 3367, JALAN AM 2 ARAB MALAYSIAN INDUSTRIAL PARK Nilai 71800, Negeri Sembilan, MY |
Product Code | LYY |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-11-09 |
Decision Date | 1995-08-18 |