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PRESSURE INDICATOR-REGULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K813577
510(k) Type
Traditional
Applicant
ADVANCED CATHETER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1982
Days to Decision
37 days

PRESSURE INDICATOR-REGULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K813577
510(k) Type
Traditional
Applicant
ADVANCED CATHETER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/1982
Days to Decision
37 days