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HEADPHONES, PATIENT ALERT, STANDALONE INTERFACE

Page Type
Cleared 510(K)
510(k) Number
K133670
510(k) Type
Abbreviated
Applicant
NEOCOIL, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2014
Days to Decision
237 days
Submission Type
Summary

HEADPHONES, PATIENT ALERT, STANDALONE INTERFACE

Page Type
Cleared 510(K)
510(k) Number
K133670
510(k) Type
Abbreviated
Applicant
NEOCOIL, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2014
Days to Decision
237 days
Submission Type
Summary