The following data is part of a premarket notification filed by Multisafe Sdn Bhd with the FDA for Multisafe-powdered Nitrile Gloves, Non-sterile (blue).
Device ID | K001497 |
510k Number | K001497 |
Device Name: | MULTISAFE-POWDERED NITRILE GLOVES, NON-STERILE (BLUE) |
Classification | Polymer 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 | LZA |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-05-15 |
Decision Date | 2000-07-26 |