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L(3), LYSNIG LEAD LATEX RADIATION GLOVE(R)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896076
510(k) Type
Traditional
Applicant
ADVANCE MEDICAL DESIGNS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/1990
Days to Decision
77 days

L(3), LYSNIG LEAD LATEX RADIATION GLOVE(R)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896076
510(k) Type
Traditional
Applicant
ADVANCE MEDICAL DESIGNS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/1990
Days to Decision
77 days