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DESERET EPIDURAL CATHETER W/TOUGHY-BORST ADAPTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850505
510(k) Type
Traditional
Applicant
PARKE-DAVIS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1985
Days to Decision
31 days

DESERET EPIDURAL CATHETER W/TOUGHY-BORST ADAPTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850505
510(k) Type
Traditional
Applicant
PARKE-DAVIS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1985
Days to Decision
31 days