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MEDIPHONIX CUSTOM FULL SHELL CUSTOM CANAL

Page Type
Cleared 510(K)
510(k) Number
K924450
510(k) Type
Traditional
Applicant
MEDIPHONIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/1992
Days to Decision
35 days
Submission Type
Statement

MEDIPHONIX CUSTOM FULL SHELL CUSTOM CANAL

Page Type
Cleared 510(K)
510(k) Number
K924450
510(k) Type
Traditional
Applicant
MEDIPHONIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/1992
Days to Decision
35 days
Submission Type
Statement