Last synced on 25 November 2022 at 11:04 pm

PILLOW MASKER, C2007M, C2008M,CE2000, WONDER EAR, MINI WONDER EAR, PT-2SM, PT-3SM, PT-3LFM, PT-3HFM, PT3CM, PT5-SM, PT5-

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982432
510(k) Type
Traditional
Applicant
TINNITUS TREATMENT CENTERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/1999
Days to Decision
196 days
Submission Type
Summary

PILLOW MASKER, C2007M, C2008M,CE2000, WONDER EAR, MINI WONDER EAR, PT-2SM, PT-3SM, PT-3LFM, PT-3HFM, PT3CM, PT5-SM, PT5-

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982432
510(k) Type
Traditional
Applicant
TINNITUS TREATMENT CENTERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/1999
Days to Decision
196 days
Submission Type
Summary