Last synced on 14 November 2025 at 11:06 pm

LATEX PATIENT EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K960942
510(k) Type
Traditional
Applicant
SIAM SEMPERMED CORP. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1996
Days to Decision
217 days
Submission Type
Summary

LATEX PATIENT EXAMINATION GLOVE

Page Type
Cleared 510(K)
510(k) Number
K960942
510(k) Type
Traditional
Applicant
SIAM SEMPERMED CORP. LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1996
Days to Decision
217 days
Submission Type
Summary