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UNIVERSAL INSTRU. SET FOR NEUROVASCULAR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831071
510(k) Type
Traditional
Applicant
PROTHIA USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1983
Days to Decision
65 days

UNIVERSAL INSTRU. SET FOR NEUROVASCULAR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831071
510(k) Type
Traditional
Applicant
PROTHIA USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/8/1983
Days to Decision
65 days