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REXTON RX12PP, RX20PP & RX34PP IN-THE-EAR HEAR AID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892333
510(k) Type
Traditional
Applicant
REXTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/1989
Days to Decision
44 days