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HIGH PRESSURE, 1 & 3 WAY STERILE DISPOS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842829
510(k) Type
Traditional
Applicant
NORTH AMERICAN INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1984
Days to Decision
90 days

HIGH PRESSURE, 1 & 3 WAY STERILE DISPOS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842829
510(k) Type
Traditional
Applicant
NORTH AMERICAN INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1984
Days to Decision
90 days