MOBILE X-RAY UNIT— 510(k) K790511
Substantially EquivalentGeneral X-Ray, Inc.
FDA 510(k) clearance K790511 for MOBILE X-RAY UNIT, Substantially Equivalent on 1979-03-26. Applicant: General X-Ray, Inc.. Device class: 2.
Clearance details
- Applicant
- General X-Ray, Inc.
- Product code
- Code IZL
- Device class
- Class 2
- Regulation
- 21 CFR 892.1720
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code IZL
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view allAdverse events under product code IZL
product code IZL- Other
- 3
- Total
- 3
Source: openFDA MAUDE database, through . 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.