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BIPOLAR ELECTROSURGICAL INTRAOCULAR PROBE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864402
510(k) Type
Traditional
Applicant
NEW ENGLAND SURGICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/1987
Days to Decision
75 days

BIPOLAR ELECTROSURGICAL INTRAOCULAR PROBE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864402
510(k) Type
Traditional
Applicant
NEW ENGLAND SURGICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/20/1987
Days to Decision
75 days