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KENTEX DISPOSABLE VAGINAL SPECULUM

Page Type
Cleared 510(K)
510(k) Number
K030693
510(k) Type
Traditional
Applicant
KENTRON HEALTH CARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2003
Days to Decision
175 days
Submission Type
Summary

KENTEX DISPOSABLE VAGINAL SPECULUM

Page Type
Cleared 510(K)
510(k) Number
K030693
510(k) Type
Traditional
Applicant
KENTRON HEALTH CARE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/2003
Days to Decision
175 days
Submission Type
Summary