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NEUROCALM MODEL 1 AND 2

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090866
510(k) Type
Traditional
Applicant
Neuromed Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2009
Days to Decision
204 days
Submission Type
Summary

NEUROCALM MODEL 1 AND 2

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090866
510(k) Type
Traditional
Applicant
Neuromed Devices, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/21/2009
Days to Decision
204 days
Submission Type
Summary