Product code JQG— Clinical Chemistry

FDA has cleared 5 devices under product code JQG between 1978 and 1981, 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.

• 19811 clearance
• 19802 clearances
• 19791 clearance
• 19781 clearance

• Ria Products, Inc.1 clearance
• Nuclear Diagnostics, Inc.1 clearance
• Mallinckrodt Critical Care1 clearance
• Immuno Assay Corp.1 clearance
• Diagnostic Corp. of America1 clearance

• K811954 — COMBO-FER IRON DIAGNOSTICImmuno Assay Corp.·1981-07-27
• K800710 — FERRITIRON KIT CAT. #RP-1100Ria Products, Inc.·1980-05-14
• K800868 — FERRO-QUANT TM FE 59 TEST KITMallinckrodt Critical Care·1980-04-29
• K790133 — SPINSEP-FE59Nuclear Diagnostics, Inc.·1979-03-02
• K780412 — TOTAL IRON BINDING CAPACITYDiagnostic Corp. of America·1978-05-26