Last synced on 30 November 2024 at 11:09 am

MT 80 SP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931040
510(k) Type
Traditional
Applicant
MAICO HEARING INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1993
Days to Decision
92 days
Submission Type
Statement