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STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVE

Page Type
Cleared 510(K)
510(k) Number
K012282
510(k) Type
Traditional
Applicant
CYPRESS MEDICAL PRODUCTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2001
Days to Decision
17 days
Submission Type
Statement

STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVE

Page Type
Cleared 510(K)
510(k) Number
K012282
510(k) Type
Traditional
Applicant
CYPRESS MEDICAL PRODUCTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2001
Days to Decision
17 days
Submission Type
Statement