MAYTEX PATIENT EXAMINATION GLOVES

Latex Patient Examination Glove

AMERICAN SEAL CO.

The following data is part of a premarket notification filed by American Seal Co. with the FDA for Maytex Patient Examination Gloves.

Pre-market Notification Details

Device IDK892553
510k NumberK892553
Device Name:MAYTEX PATIENT EXAMINATION GLOVES
ClassificationLatex Patient Examination Glove
Applicant AMERICAN SEAL CO. 25029 VIKING ST. Hayward,  CA  94545
ContactBrian Hsu
CorrespondentBrian Hsu
AMERICAN SEAL CO. 25029 VIKING ST. Hayward,  CA  94545
Product CodeLYY  
CFR Regulation Number880.6250 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1989-04-10
Decision Date1989-05-25

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.