Product code KEQ— Pathology

FDA has cleared 7 devices under product code KEQ between 1978 and 1983, filed by 4 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.

• 19831 clearance
• 19803 clearances
• 19783 clearances

• Meridian Diagnostics, Inc.3 clearances
• Marion Laboratories, Inc.2 clearances
• Surgipath Medical Industries, Inc.1 clearance
• Flow Laboratories, Inc.1 clearance

• K830515 — SCOTTS TAP WATER SUBSTITUTE CONCENTRATESurgipath Medical Industries, Inc.·1983-03-31
• K792702 — VASPAR SEALANTMeridian Diagnostics, Inc.·1980-01-24
• K792703 — LACTO-PHENOL ANALINE BLUE FLUIDMeridian Diagnostics, Inc.·1980-01-24
• K792709 — KOH MOUNTING FLUID W/GLYCEROLMeridian Diagnostics, Inc.·1980-01-24
• K781868 — DROPPER, CEPTI-SEAL LAVTOPHENOLMarion Laboratories, Inc.·1978-11-22
• K781869 — DROPPER, CEPTI-SEAL KOH SOLUTIONMarion Laboratories, Inc.·1978-11-22
• K781388 — F.A. MOUNTING MEDIUMFlow Laboratories, Inc.·1978-08-21