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CYPRESS MEDICAL PRODUCTS STERILE LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K950254
510(k) Type
Traditional
Applicant
CYPRESS MEDICAL PRODUCTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1995
Days to Decision
67 days
Submission Type
Statement

CYPRESS MEDICAL PRODUCTS STERILE LATEX EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K950254
510(k) Type
Traditional
Applicant
CYPRESS MEDICAL PRODUCTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/1995
Days to Decision
67 days
Submission Type
Statement