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STERILE, POWDERFREE LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K980785
510(k) Type
Traditional
Applicant
LONDON INTL. LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1998
Days to Decision
100 days
Submission Type
Statement

STERILE, POWDERFREE LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K980785
510(k) Type
Traditional
Applicant
LONDON INTL. LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1998
Days to Decision
100 days
Submission Type
Statement