The following data is part of a premarket notification filed by Yty Industry (manjung) Sdn. Bhd. with the FDA for Non-sterile, Powder-free Nitrile Blue & White Examination Gloves.
Device ID | K052502 |
510k Number | K052502 |
Device Name: | NON-STERILE, POWDER-FREE NITRILE BLUE & WHITE EXAMINATION GLOVES |
Classification | Polymer Patient Examination Glove |
Applicant | YTY INDUSTRY (MANJUNG) SDN. BHD. 198 AVENUE DE LA D'EMERALD Sparks, NV 89434 -9550 |
Contact | Janna P Tucker |
Correspondent | Janna P Tucker YTY INDUSTRY (MANJUNG) SDN. BHD. 198 AVENUE DE LA D'EMERALD Sparks, NV 89434 -9550 |
Product Code | LZA |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-09-13 |
Decision Date | 2005-11-18 |
Summary: | summary |