The following data is part of a premarket notification filed by Shen Wei (usa), Inc. with the FDA for Powder-free Latex Examination Gloves With Aloe And Protein Claim, Tested For Use With Chemotherapy Drugs.
Device ID | K013794 |
510k Number | K013794 |
Device Name: | POWDER-FREE LATEX EXAMINATION GLOVES WITH ALOE AND PROTEIN CLAIM, TESTED FOR USE WITH CHEMOTHERAPY DRUGS |
Classification | Latex Patient Examination Glove |
Applicant | SHEN WEI (USA), INC. 2845 WHIPPLE RD. Union City, CA 94587 |
Contact | Belle L Chou |
Correspondent | Belle L Chou SHEN WEI (USA), INC. 2845 WHIPPLE RD. Union City, CA 94587 |
Product Code | LYY |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-11-14 |
Decision Date | 2002-01-22 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
20304040132207 | K013794 | 000 |
20304040132191 | K013794 | 000 |
20304040132184 | K013794 | 000 |
20304040132177 | K013794 | 000 |
20304040004658 | K013794 | 000 |