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SEAMLESS LATEX PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K891491
510(k) Type
Traditional
Applicant
DIGITCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/1989
Days to Decision
53 days

SEAMLESS LATEX PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K891491
510(k) Type
Traditional
Applicant
DIGITCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/1989
Days to Decision
53 days