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OMNITECH RESECTOSCOPE ROLLER ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K965093
510(k) Type
Traditional
Applicant
OMNITECH SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1997
Days to Decision
90 days
Submission Type
Statement

OMNITECH RESECTOSCOPE ROLLER ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K965093
510(k) Type
Traditional
Applicant
OMNITECH SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1997
Days to Decision
90 days
Submission Type
Statement