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EXTEND-EAR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920466
510(k) Type
Traditional
Applicant
SONOVATION, INC. DBA AVR SONOVATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/1992
Days to Decision
31 days
Submission Type
Statement