GE Healthcare · Nuclear MedicineInfiniaMillenniumDiscovery
FDA Regulations require that 21CFR1020.30 and 21CFR1020.30 information about X-ray emitting systems is provided to the u…
FDA Regulations require that 21CFR1020.30 and 21CFR1020.30 information about X-ray emitting systems is provided to the user, in the User Documentation
Symptom
FDA Regulations require that 21CFR1020.30 and 21CFR1020.30 information about X-ray emitting systems is provided to the user, in the User Documentation FDA Regulations require that 21CFR1020.30 and 21CFR1020.30 information about X-ray emitting systems is provided to the user, in the User Documentation.
Applies to
- Models
- Infinia, Millennium, Discovery
- Product
- Infinia II Infinia II Acquisition System Infinia I Infinia I Acquisition System VGH VG and VG Hawkey and Varicam Infinia HE4 Infinia II Hawkeye 4 & Infinia II GP (Infinia running Windows XP software)
- Component
- *X-Ray (Generator, DAS, Controller) *X-Ray (Generator, DAS, Controller)
- Area
- Nuclear Medicine
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