Product code IYZ— Radiology
CARDIAC SPECT PALLET
- Classification name
- Bed, Scanning, Nuclear
- Device class
- Class 1
- Regulation
- 21 CFR 892.1350
- Advisory panel
- Radiology
- Total cleared
- 12
- First cleared
- Most recent
Market context for product code IYZ
FDA has cleared devices under product code IYZ between 1989 and 1992, filed by 5 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1992
- 1991
- 1990
- 1989
Top applicants under product code IYZ
Recent clearances under product code IYZ
- K920962 — MULTIPLE ACCESSORY TO GAMMA CAMERAS
- K915541 — SPECT TABLE, MODEL #056-760
- K911691 — XYZ CRANK IMAGING TABLE
- K912286 — CARDIAC SPECT PALLET
- K912481 — ECT CARBON FIBER PALLET, MODIFICATION
- K912135 — XY IMAGING TABLE
- K912181 — E-Z LIFT CRANK IMAGING TABLE
- K911561 — XYZ IMAGING TABLE WITH FOOT PUMP
- K911564 — E-Z LIFT IMAGING TABLE WITH FOOT PUMP
- K903901 — SCANNING COT
- K903767 — ECT (EMMISSION COMPUTED TOMOGRAPHY) CARBON FIB PAL
- K893826 — QRSYSTEMS H.D. NUCLEAR IMAGING TABLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.