Last synced on 19 April 2024 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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