The following data is part of a premarket notification filed by Safeskin Retailing (hk) Limited with the FDA for White Nitrile Powder Free Patient Examination Glove, Non Sterile.
Device ID | K222713 |
510k Number | K222713 |
Device Name: | White Nitrile Powder Free Patient Examination Glove, Non Sterile |
Classification | Polymer Patient Examination Glove |
Applicant | Safeskin Retailing (HK) Limited 26th Floor, Beautiful Group Tower, 77 Connaught Road Central Hong Kong, CN |
Contact | Alvin Ho |
Correspondent | Stephan Toupan Dawa Medical LLC 7320 NW 12th Street Suite 103 Miami, FL 33126 |
Product Code | LZA |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2022-09-08 |
Decision Date | 2022-12-03 |