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INVASIVE MONITORING KITS

Page Type
Cleared 510(K)
510(k) Number
K832907
510(k) Type
Traditional
Applicant
AMERICAN PHARMASEAL DIV. AHSC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1984
Days to Decision
134 days

INVASIVE MONITORING KITS

Page Type
Cleared 510(K)
510(k) Number
K832907
510(k) Type
Traditional
Applicant
AMERICAN PHARMASEAL DIV. AHSC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1984
Days to Decision
134 days