Last synced on 30 May 2025 at 11:05 pm

CREATINE KINASE-MB TEST (CK-MK) ITEM NUMBER 65673

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884547
510(k) Type
Traditional
Applicant
EM DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1989
Days to Decision
102 days

CREATINE KINASE-MB TEST (CK-MK) ITEM NUMBER 65673

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884547
510(k) Type
Traditional
Applicant
EM DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1989
Days to Decision
102 days