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IREX CARDIOPLAN

Page Type
Cleared 510(K)
510(k) Number
K792525
510(k) Type
Traditional
Applicant
IREX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/1979
Days to Decision
21 days

IREX CARDIOPLAN

Page Type
Cleared 510(K)
510(k) Number
K792525
510(k) Type
Traditional
Applicant
IREX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/1979
Days to Decision
21 days