Last synced on 4 February 2023 at 10:33 pm

MM-CE DM (BEHIND THE EAR)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K780921
510(k) Type
Traditional
Applicant
ARGOSY INTL. (USA), INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/14/1978
Days to Decision
9 days