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600 & 900 SERIES ELECTRODES & 755 & 756 HANDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K885200
510(k) Type
Traditional
Applicant
OLSEN ELECTROSURGICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/1989
Days to Decision
28 days

600 & 900 SERIES ELECTRODES & 755 & 756 HANDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K885200
510(k) Type
Traditional
Applicant
OLSEN ELECTROSURGICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/1989
Days to Decision
28 days