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CLASSIC ECG/STIMULATING NO. 1700 SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900519
510(k) Type
Traditional
Applicant
CLASSIC MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1990
Days to Decision
45 days

CLASSIC ECG/STIMULATING NO. 1700 SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900519
510(k) Type
Traditional
Applicant
CLASSIC MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1990
Days to Decision
45 days