Last synced on 14 November 2025 at 11:06 pm

CARDIOINTEGRAM

Page Type
Cleared 510(K)
510(k) Number
K812971
510(k) Type
Traditional
Applicant
OCG TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1981
Days to Decision
68 days

CARDIOINTEGRAM

Page Type
Cleared 510(K)
510(k) Number
K812971
510(k) Type
Traditional
Applicant
OCG TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1981
Days to Decision
68 days