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ACCUFIX RADIOLUCENT PELVIS AND BELLY BOARDS, ACCUFIX CANTILEVER HEAD BOARD WITH SHOULDER DEPRESSION, ACCUFIX RADIOLUCENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032156
510(k) Type
Traditional
Applicant
WFR/AQUAPLAST CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2003
Days to Decision
50 days
Submission Type
Statement

ACCUFIX RADIOLUCENT PELVIS AND BELLY BOARDS, ACCUFIX CANTILEVER HEAD BOARD WITH SHOULDER DEPRESSION, ACCUFIX RADIOLUCENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032156
510(k) Type
Traditional
Applicant
WFR/AQUAPLAST CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2003
Days to Decision
50 days
Submission Type
Statement