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OMNITRON GYN APPLICATOR SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913908
510(k) Type
Traditional
Applicant
OMNITRON INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/1992
Days to Decision
189 days
Submission Type
Statement

OMNITRON GYN APPLICATOR SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913908
510(k) Type
Traditional
Applicant
OMNITRON INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/1992
Days to Decision
189 days
Submission Type
Statement