Last synced on 2 May 2025 at 11:05 pm

CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900246
510(k) Type
Traditional
Applicant
PPG INDUSTRIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/1990
Days to Decision
167 days

CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900246
510(k) Type
Traditional
Applicant
PPG INDUSTRIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/1990
Days to Decision
167 days