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PHF20 20 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
K935580
510(k) Type
Traditional
Applicant
PRECISE OPTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1994
Days to Decision
118 days
Submission Type
Statement

PHF20 20 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
K935580
510(k) Type
Traditional
Applicant
PRECISE OPTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1994
Days to Decision
118 days
Submission Type
Statement