Last synced on 23 September 2022 at 11:05 pm

SIEMENS FRONTIER SERICE, MODELS S-1,S-2 AND S-3 MULTIPLE SITUATION, SINGLE CHANNEL PROGRAMMABLE INSTRUMENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K944645
510(k) Type
Traditional
Applicant
SIEMENS HEARING INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/1994
Days to Decision
97 days
Submission Type
Summary