Product code KQS— Gastroenterology, Urology

FDA has cleared 8 devices under product code KQS between 1976 and 1995, filed by 6 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.

• 19951 clearance
• 19871 clearance
• 19862 clearances
• 19851 clearance
• 19801 clearance
• 19791 clearance
• 19761 clearance

• Mallinckrodt Group, Inc.2 clearances
• American Sterilizer Co.2 clearances
• Sybron Corp.1 clearance
• Siemens Corp.1 clearance
• Oec-Diasonics, Inc.1 clearance
• Dornier Medtech America, Inc.1 clearance

• K955019 — UROTRACT IDornier Medtech America, Inc.·1995-12-06
• K872022 — UROVIEWOec-Diasonics, Inc.·1987-07-16
• K864846 — RADIOGRAPHIC - LEG SECTIONAmerican Sterilizer Co.·1986-12-24
• K860040 — HYDRAJUST III UROLOGICAL TABLEMallinckrodt Group, Inc.·1986-02-10
• K852127 — AMSCO URO-ENDO MOBILE TABLEAmerican Sterilizer Co.·1985-08-08
• K801723 — UR 150-UR 150TSiemens Corp.·1980-08-13
• K791699 — HYDRADJUST II UROLOGICAL TABLESybron Corp.·1979-10-22
• K760522 — TABLE, UROSURGICALMallinckrodt Group, Inc.·1976-12-16