The following data is part of a premarket notification filed by Brightsway Holdings Sdn Bhd with the FDA for Brightway Brand Blue Color Latex Examination Glove, Powder Free Containing 50 Mlgm Or Less Of Water Extractable Protein.
Device ID | K991750 |
510k Number | K991750 |
Device Name: | BRIGHTWAY BRAND BLUE COLOR LATEX EXAMINATION GLOVE, POWDER FREE CONTAINING 50 MLGM OR LESS OF WATER EXTRACTABLE PROTEIN |
Classification | Latex Patient Examination Glove |
Applicant | BRIGHTSWAY HOLDINGS SDN BHD BATU BELAH Klang Selangor Darul Ehsan, MY 42100 |
Contact | G. Baskaran |
Correspondent | G. Baskaran BRIGHTSWAY HOLDINGS SDN BHD BATU BELAH Klang Selangor Darul Ehsan, MY 42100 |
Product Code | LYY |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-05-24 |
Decision Date | 1999-06-23 |