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ELECTROSURGICAL GENERATOR MODEL ESU100/250/550

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914367
510(k) Type
Traditional
Applicant
GYNE-TECH INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1992
Days to Decision
210 days
Submission Type
Summary

ELECTROSURGICAL GENERATOR MODEL ESU100/250/550

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914367
510(k) Type
Traditional
Applicant
GYNE-TECH INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1992
Days to Decision
210 days
Submission Type
Summary