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P1806 MOBILE C-ARM IMAGE INTENSIFIER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K792225
510(k) Type
Traditional
Applicant
PRECISE OPTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1979
Days to Decision
45 days

P1806 MOBILE C-ARM IMAGE INTENSIFIER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K792225
510(k) Type
Traditional
Applicant
PRECISE OPTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1979
Days to Decision
45 days