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PATIENT EXAMINATION GLOVE (LATEX)

Page Type
Cleared 510(K)
510(k) Number
K891980
510(k) Type
Traditional
Applicant
MONTROSE INTL., CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1989
Days to Decision
30 days

PATIENT EXAMINATION GLOVE (LATEX)

Page Type
Cleared 510(K)
510(k) Number
K891980
510(k) Type
Traditional
Applicant
MONTROSE INTL., CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1989
Days to Decision
30 days