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EEG REAL PATIENT SPIKE AND EVENT DETECTOR MODULE, MODEL EX-SP-RP (PROPOSED)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010085
510(k) Type
Traditional
Applicant
Excel Tech. , Ltd.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
3/15/2001
Days to Decision
63 days
Submission Type
Summary

EEG REAL PATIENT SPIKE AND EVENT DETECTOR MODULE, MODEL EX-SP-RP (PROPOSED)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010085
510(k) Type
Traditional
Applicant
Excel Tech. , Ltd.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
3/15/2001
Days to Decision
63 days
Submission Type
Summary