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KENTEX DISPOSABLE VAGINAL SPECULUM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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