The following data is part of a premarket notification filed by Wrp Specialty Products Sdn. Bhd. with the FDA for Dermagrip Powder Free Nitrile Examination Glove, Non Sterile.
Device ID | K990752 |
510k Number | K990752 |
Device Name: | DERMAGRIP POWDER FREE NITRILE EXAMINATION GLOVE, NON STERILE |
Classification | Polymer Patient Examination Glove |
Applicant | WRP SPECIALTY PRODUCTS SDN. BHD. LOT11, JL.2,KAWASAN PERUSAHAAN BANDAR BARU SLAK TINGGI Selangor Daurl Ehsan, Sepang, MY 43900 |
Contact | Cheng Hean Khoo |
Correspondent | Cheng Hean Khoo WRP SPECIALTY PRODUCTS SDN. BHD. LOT11, JL.2,KAWASAN PERUSAHAAN BANDAR BARU SLAK TINGGI Selangor Daurl Ehsan, Sepang, MY 43900 |
Product Code | LZA |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-03-08 |
Decision Date | 1999-10-18 |
Summary: | summary |