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PORTABLE X-RAY SYSTEM, MODEL POWERMAX 1260

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090655
510(k) Type
Traditional
Applicant
Source-Ray, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2009
Days to Decision
125 days
Submission Type
Statement

PORTABLE X-RAY SYSTEM, MODEL POWERMAX 1260

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090655
510(k) Type
Traditional
Applicant
Source-Ray, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/2009
Days to Decision
125 days
Submission Type
Statement