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ANTELOPE BRAND PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K892781
510(k) Type
Traditional
Applicant
LIAONING-USA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/1989
Days to Decision
163 days

ANTELOPE BRAND PATIENT EXAMINATION GLOVES

Page Type
Cleared 510(K)
510(k) Number
K892781
510(k) Type
Traditional
Applicant
LIAONING-USA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/21/1989
Days to Decision
163 days