The following data is part of a premarket notification filed by Multisafe Sdn Bhd with the FDA for Blue Powdered Latex Examination Gloves, Non-sterile.
Device ID | K062526 |
510k Number | K062526 |
Device Name: | BLUE POWDERED LATEX EXAMINATION GLOVES, NON-STERILE |
Classification | Latex Patient Examination Glove |
Applicant | MULTISAFE SDN BHD LOT 764 BIDOR INDUSTRIAL ESTATE Bidor, Perak, MY 35500 |
Contact | Abd Hadi Bin Husin |
Correspondent | Abd Hadi Bin Husin MULTISAFE SDN BHD LOT 764 BIDOR INDUSTRIAL ESTATE Bidor, Perak, MY 35500 |
Product Code | LYY |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-08-28 |
Decision Date | 2007-04-13 |
Summary: | summary |