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ELECTROSURGICAL COAGULATION SUCTION TUBE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895337
510(k) Type
Traditional
Applicant
NEW ENGLAND SURGICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1989
Days to Decision
16 days

ELECTROSURGICAL COAGULATION SUCTION TUBE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895337
510(k) Type
Traditional
Applicant
NEW ENGLAND SURGICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1989
Days to Decision
16 days