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MICROGYN RESECTION LOOP, COAGULATING ELECTRODE, CISS SHEATH ELECTRODE, LOOP ELECTRODE KIT AND COAGULATING ELECTRODE KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962653
510(k) Type
Traditional
Applicant
Microgyn Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1997
Days to Decision
211 days
Submission Type
Statement

MICROGYN RESECTION LOOP, COAGULATING ELECTRODE, CISS SHEATH ELECTRODE, LOOP ELECTRODE KIT AND COAGULATING ELECTRODE KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962653
510(k) Type
Traditional
Applicant
Microgyn Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1997
Days to Decision
211 days
Submission Type
Statement