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SKINSENSE NITRILE POWDER-FREE SYNTHETIC MEDICAL EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984249
510(k) Type
Traditional
Applicant
LONDON INTERNATIONAL GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1999
Days to Decision
155 days
Submission Type
Statement

SKINSENSE NITRILE POWDER-FREE SYNTHETIC MEDICAL EXAMINATION GLOVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984249
510(k) Type
Traditional
Applicant
LONDON INTERNATIONAL GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/1999
Days to Decision
155 days
Submission Type
Statement