STERILE PATIENT EXAMINATION GLOVE

Latex Patient Examination Glove

BOSTON MEDICAL CORP.

The following data is part of a premarket notification filed by Boston Medical Corp. with the FDA for Sterile Patient Examination Glove.

Pre-market Notification Details

Device IDK891103
510k NumberK891103
Device Name:STERILE PATIENT EXAMINATION GLOVE
ClassificationLatex Patient Examination Glove
Applicant BOSTON MEDICAL CORP. 8350 BRISTOL COURT SUITE 101 Jessup,  MD  20794
ContactTimothy F Hand
CorrespondentTimothy F Hand
BOSTON MEDICAL CORP. 8350 BRISTOL COURT SUITE 101 Jessup,  MD  20794
Product CodeLYY  
CFR Regulation Number880.6250 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1989-02-17
Decision Date1989-03-14

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