Last synced on 4 February 2023 at 10:33 pm

MODEL FM5

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831371
510(k) Type
Traditional
Applicant
SONICAID, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1983
Days to Decision
64 days

MODEL FM5

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K831371
510(k) Type
Traditional
Applicant
SONICAID, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1983
Days to Decision
64 days