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BWII EEG DIGITAL, MODEL PV 1652; BWII PSG DIGITAL, MODEL PV 1524

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062533
510(k) Type
Traditional
Applicant
NEUROVIRTUAL USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2006
Days to Decision
115 days
Submission Type
Summary

BWII EEG DIGITAL, MODEL PV 1652; BWII PSG DIGITAL, MODEL PV 1524

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062533
510(k) Type
Traditional
Applicant
NEUROVIRTUAL USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2006
Days to Decision
115 days
Submission Type
Summary