Last synced on 14 November 2025 at 11:06 pm

DEEP CANAL HEARING INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K942702
510(k) Type
Traditional
Applicant
REXTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/1994
Days to Decision
196 days
Submission Type
Summary

DEEP CANAL HEARING INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K942702
510(k) Type
Traditional
Applicant
REXTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/1994
Days to Decision
196 days
Submission Type
Summary