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EARPOPPER, MODEL EP-2000, EP-2100, EP-3000

Page Type
Cleared 510(K)
510(k) Number
K073401
510(k) Type
Traditional
Applicant
Micromedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/2008
Days to Decision
101 days
Submission Type
Summary

EARPOPPER, MODEL EP-2000, EP-2100, EP-3000

Page Type
Cleared 510(K)
510(k) Number
K073401
510(k) Type
Traditional
Applicant
Micromedics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/14/2008
Days to Decision
101 days
Submission Type
Summary