Last synced on 20 December 2024 at 11:05 pm

MTHF-9S MOBIL C-ARM IMAGE INTENSIFIER UNIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900194
510(k) Type
Traditional
Applicant
IMT AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/1990
Days to Decision
111 days

MTHF-9S MOBIL C-ARM IMAGE INTENSIFIER UNIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900194
510(k) Type
Traditional
Applicant
IMT AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/7/1990
Days to Decision
111 days