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UNIMAX ITE & ULTRAMAX-CCR CUSTOM CANAL INSTRUMENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864277
510(k) Type
Traditional
Applicant
UNIMAX HEARING INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1987
Days to Decision
71 days