Product code KQW— Orthopedic

FDA has cleared 13 devices under product code KQW between 1976 and 1993, 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.

• 19931 clearance
• 19901 clearance
• 19871 clearance
• 19851 clearance
• 19831 clearance
• 19812 clearances
• 19804 clearances
• 19762 clearances

• Fred Sammons, Inc.8 clearances
• Twin City Surgical, Inc.1 clearance
• The Telos Co.1 clearance
• Sgarlato Laboratories, Inc.1 clearance
• Chattanooga Group, Inc.1 clearance
• Biosearch Medical Products, Inc.1 clearance

• K926237 — O'BRIEN GONIOMETERSgarlato Laboratories, Inc.·1993-08-02
• K901744 — DOBBHOFF(R) RETRIEVAL FORCEPSBiosearch Medical Products, Inc.·1990-07-03
• K870767 — THE (CROM) TESTERTwin City Surgical, Inc.·1987-03-17
• K850082 — HAND HELD GONIOMETERChattanooga Group, Inc.·1985-04-04
• K831550 — FINGER BONIOMETER BK7506Fred Sammons, Inc.·1983-06-24
• K812778 — THE TELOS EQUIPMENTThe Telos Co.·1981-12-08
• K810441 — UNIVERSAL GONIMETERFred Sammons, Inc.·1981-02-27
• K801715 — BK-7497 BULB DYNAMOMETERFred Sammons, Inc.·1980-08-04
• K801716 — BK-7505 RADIOPAQUE GONIOMETER, 8Fred Sammons, Inc.·1980-08-04
• K801717 — BK-7511 BRASS GONIOMETERFred Sammons, Inc.·1980-08-04
• K801718 — BK-7513 STAINLESS STEEL GONIOMETERFred Sammons, Inc.·1980-08-04
• K760301 — GONIOMETER, MED. INTER. STAND. BK-7512Fred Sammons, Inc.·1976-09-08
• K760302 — GONIOMETER, INTER. STAND. LARGE, BK7514Fred Sammons, Inc.·1976-09-08