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SOMNITOR 32K SLEEP ACTIVITY MONITOR

Page Type
Cleared 510(K)
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)
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