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SENSI-DERM LATEX SURGICAL GLOVES (POWDERED)

Page Type
Cleared 510(K)
510(k) Number
K980880
510(k) Type
Traditional
Applicant
ANSELL PERRY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/1998
Days to Decision
72 days
Submission Type
Summary

SENSI-DERM LATEX SURGICAL GLOVES (POWDERED)

Page Type
Cleared 510(K)
510(k) Number
K980880
510(k) Type
Traditional
Applicant
ANSELL PERRY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/1998
Days to Decision
72 days
Submission Type
Summary