Last synced on 27 January 2023 at 11:04 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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