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ELECTROSURGICAL CUTTING/COAGULATION DEVICE/ACCESS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914066
510(k) Type
Traditional
Applicant
LAPAROMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/1991
Days to Decision
57 days
Submission Type
Statement

ELECTROSURGICAL CUTTING/COAGULATION DEVICE/ACCESS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914066
510(k) Type
Traditional
Applicant
LAPAROMED CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/1991
Days to Decision
57 days
Submission Type
Statement