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RIONET HEARING AID HB-52AS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915319
510(k) Type
Traditional
Applicant
RION CO. LTD. DBA RION ACOUSTIC DEVICE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1992
Days to Decision
48 days
Submission Type
Statement