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PATIENT EXAMINATION GLOVES (LATEX)

Page Type
Cleared 510(K)
510(k) Number
K891637
510(k) Type
Traditional
Applicant
POWERCREST (M) SDN. BHD.
Country
Malaysia
FDA Decision
Substantially Equivalent
Decision Date
4/14/1989
Days to Decision
28 days

PATIENT EXAMINATION GLOVES (LATEX)

Page Type
Cleared 510(K)
510(k) Number
K891637
510(k) Type
Traditional
Applicant
POWERCREST (M) SDN. BHD.
Country
Malaysia
FDA Decision
Substantially Equivalent
Decision Date
4/14/1989
Days to Decision
28 days