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MTHF-9R 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
K900193
510(k) Type
Traditional
Applicant
IMT AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1990
Days to Decision
113 days

MTHF-9R 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
K900193
510(k) Type
Traditional
Applicant
IMT AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1990
Days to Decision
113 days