Product code KOQ— Dental

FDA has cleared 4 devices under product code KOQ between 1983 and 1990, filed by 3 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.

• 19903 clearances
• 19831 clearance

• North American Sterilization & Packaging Co.2 clearances
• Uresil Corp.1 clearance
• Solar Dental Co., Inc.1 clearance

• K901882 — URESIL ENDOSCOPIC LASER OVERTUBEUresil Corp.·1990-07-27
• K896821 — OLYMPUS URETERO. & CIRCON ACMI URETERO. GUIDENorth American Sterilization & Packaging Co.·1990-02-09
• K900401 — NAS&P GRASPING FORCEPS & ASSOC. DEVICESNorth American Sterilization & Packaging Co.·1990-02-09
• K831265 — DENTOLOCK DENTURE ADHESIVE CREAMSolar Dental Co., Inc.·1983-05-09