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MODEL 6000FD AMBULATORY ECG ANALYSIS SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K873680
510(k) Type
Traditional
Applicant
OXFORD MEDILOG, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/1987
Days to Decision
70 days

MODEL 6000FD AMBULATORY ECG ANALYSIS SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K873680
510(k) Type
Traditional
Applicant
OXFORD MEDILOG, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/1987
Days to Decision
70 days