Product code KYA— Obstetrics/Gynecology

FDA has cleared 5 devices under product code KYA between 1982 and 1990, 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.

• 19901 clearance
• 19841 clearance
• 19823 clearances

• American Thermometer Company, Inc.2 clearances
• Promedex, Inc.1 clearance
• Dr. John D. Reid B.A., D.C.1 clearance
• Bcsi Laboratories, Inc.1 clearance

• K900404 — VARICOSCREEN(TM)Promedex, Inc.·1990-12-07
• K832989 — BREAST THERMAL ACTIVITY INDICATORBcsi Laboratories, Inc.·1984-01-17
• K823245 — THERMAX; THERMAX SYSTEMAmerican Thermometer Company, Inc.·1982-11-16
• K821524 — CHIROPRATIC INFRA-RED CRYSTAL PAKDr. John D. Reid B.A., D.C.·1982-09-08
• K821049 — PARATHERMAmerican Thermometer Company, Inc.·1982-04-29