ACCUFIX RADIOLUCENT PELVIS AND BELLY BOARDS, ACCUFIX CANTILEVER HEAD BOARD WITH SHOULDER DEPRESSION, ACCUFIX RADIOLUCENT— 510(k) K032156

Substantially Equivalent

Wfr/Aquaplast Corp.

FDA 510(k) clearance K032156 for ACCUFIX RADIOLUCENT PELVIS AND BELLY BOARDS, ACCUFIX CANTILEVER HEAD BOARD WITH SHOULDER DEPRESSION, ACCUFIX RADIOLUCENT, Substantially Equivalent on 2003-09-02. Applicant: Wfr/Aquaplast Corp..

Clearance details

Applicant: Wfr/Aquaplast Corp.
Product code: Code IYE
Advisory panel: Radiology
Date received: 2003-07-14
Decision date: 2003-09-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wyckoff, NJ, US

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Adverse events under product code IYE

product code IYE

Malfunction: 455
Other: 3
Total: 458

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.