The following data is part of a premarket notification filed by Kilang Barangan Getah Dioh with the FDA for Powder Free Latex Examination Gloves, Non-sterile.
Device ID | K984127 |
510k Number | K984127 |
Device Name: | POWDER FREE LATEX EXAMINATION GLOVES, NON-STERILE |
Classification | Latex Patient Examination Glove |
Applicant | KILANG BARANGAN GETAH DIOH LOT 9, KAWASAN PERINDUSTRIAN DIOH, KUALA PILAH Negeri Sembilan, MY 72000 |
Contact | Norli Maniff |
Correspondent | Norli Maniff KILANG BARANGAN GETAH DIOH LOT 9, KAWASAN PERINDUSTRIAN DIOH, KUALA PILAH Negeri Sembilan, MY 72000 |
Product Code | LYY |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-11-18 |
Decision Date | 1999-01-25 |