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SOMNITOR 32K SLEEP ACTIVITY MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K965079
510(k) Type
Traditional
Applicant
NEURIM PHARMACEUTICALS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/1997
Days to Decision
203 days
Submission Type
Summary

SOMNITOR 32K SLEEP ACTIVITY MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K965079
510(k) Type
Traditional
Applicant
NEURIM PHARMACEUTICALS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/1997
Days to Decision
203 days
Submission Type
Summary