Product code KXH— Radiology

FDA has cleared 9 devices under product code KXH between 1982 and 2012, 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.

• 20121 clearance
• 19951 clearance
• 19941 clearance
• 19932 clearances
• 19891 clearance
• 19861 clearance
• 19841 clearance
• 19821 clearance

• Spectrum X-Ray Corp.3 clearances
• Octostop, Inc.3 clearances
• Ge Healthcare Coils (Usa Instruments, Inc.)1 clearance
• Fischer Imaging Corp.1 clearance
• Ar Custom Medical Products, Ltd.1 clearance

• K122174 — PEDIATRIC POSITIONER PAD SETGe Healthcare Coils (Usa Instruments, Inc.)·2012-11-16
• K953246 — OCTOROLLOctostop, Inc.·1995-09-29
• K930124 — VARIANT OF OCTOSTOP AND OCTOPAQUEOctostop, Inc.·1994-02-09
• K933134 — SPECTRUM DG-P7000 PEDIATRIC CRADLESpectrum X-Ray Corp.·1993-10-07
• K930357 — ACCESSORY TO UNIVERSAL OCTOPAQUEOctostop, Inc.·1993-07-13
• K884292 — STRETCHER TABLEFischer Imaging Corp.·1989-03-31
• K863890 — MAMM-AIREAr Custom Medical Products, Ltd.·1986-10-14
• K840463 — DIGITAL CRADLESpectrum X-Ray Corp.·1984-02-21
• K813561 — SPECTRUM PEDIATRIC CARDLE TABLESpectrum X-Ray Corp.·1982-01-29