PATIENT INFORMATION MANAGER (PIM)— 510(k) K921986
Substantially EquivalentContinental X-Ray Corp.
FDA 510(k) clearance K921986 for PATIENT INFORMATION MANAGER (PIM), Substantially Equivalent on 1992-10-16. Applicant: Continental X-Ray Corp.. Device class: 2.
Clearance details
- Applicant
- Continental X-Ray Corp.
- Product code
- Code IZH
- Device class
- Class 2
- Regulation
- 21 CFR 892.1710
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Broadview, IL, US
Recent devices under product code IZH
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- K962140 — ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300
- K961690 — CARDIOARC SERIES: POSITIONER C-ARM MODELS NO. 6896.001 AND 6896.105
- K954581 — ARC SERIES
- K950571 — LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270
Data sourced from openFDA. This site is unofficial and independent of the FDA.