Last synced on 2 December 2022 at 11:04 pm

Otowave 202 Portable Tympanometer

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150163
510(k) Type
Traditional
Applicant
AMPLIVOX, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/23/2015
Days to Decision
87 days
Submission Type
Summary

Otowave 202 Portable Tympanometer

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150163
510(k) Type
Traditional
Applicant
AMPLIVOX, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
4/23/2015
Days to Decision
87 days
Submission Type
Summary