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SHERIDAN ELECTROSURGERY PROTECTION FILTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881293
510(k) Type
Traditional
Applicant
SHERIDAN CATHETER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/1988
Days to Decision
80 days

SHERIDAN ELECTROSURGERY PROTECTION FILTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881293
510(k) Type
Traditional
Applicant
SHERIDAN CATHETER CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/1988
Days to Decision
80 days