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PATIENT EXAMINATION GLOVES (LATEX)

Page Type
Cleared 510(K)
510(k) Number
K892032
510(k) Type
Traditional
Applicant
ALIZOR, INC. DBA GLOBAL TECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1989
Days to Decision
132 days

PATIENT EXAMINATION GLOVES (LATEX)

Page Type
Cleared 510(K)
510(k) Number
K892032
510(k) Type
Traditional
Applicant
ALIZOR, INC. DBA GLOBAL TECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/10/1989
Days to Decision
132 days