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FDA 510(k) Applications Submitted by CONTINENTAL X-RAY CORP.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K961690
05/01/1996
CARDIOARC SERIES: POSITIONER C-ARM MODELS NO. 6896.001 AND 6896.105
CONTINENTAL X-RAY CORP.
K962140
06/03/1996
ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300
CONTINENTAL X-RAY CORP.
K972442
06/30/1997
CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002
CONTINENTAL X-RAY CORP.
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