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Otowave 302 Portable Tympanometer

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171265
510(k) Type
Traditional
Applicant
Amplivox Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/28/2017
Days to Decision
88 days
Submission Type
Summary

Otowave 302 Portable Tympanometer

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171265
510(k) Type
Traditional
Applicant
Amplivox Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
7/28/2017
Days to Decision
88 days
Submission Type
Summary