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RESECTOSCOPE CUTTING LOOP ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964365
510(k) Type
Traditional
Applicant
OMNITECH SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/1997
Days to Decision
172 days
Submission Type
Statement

RESECTOSCOPE CUTTING LOOP ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K964365
510(k) Type
Traditional
Applicant
OMNITECH SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/1997
Days to Decision
172 days
Submission Type
Statement