Last synced on 10 January 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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