The following data is part of a premarket notification filed by Maytex Corp. with the FDA for Maytex Latex Examination Gloves.
Device ID | K892183 |
510k Number | K892183 |
Device Name: | MAYTEX LATEX EXAMINATION GLOVES |
Classification | Latex Patient Examination Glove |
Applicant | MAYTEX CORP. 25029 VIKING ST. Hayward, CA 94545 |
Contact | Brian Hsu |
Correspondent | Brian Hsu MAYTEX CORP. 25029 VIKING ST. Hayward, CA 94545 |
Product Code | LYY |
CFR Regulation Number | 880.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-04-05 |
Decision Date | 1989-05-31 |