Product code HCB— Neurology

FDA has cleared 6 devices under product code HCB between 1976 and 1994, filed by 6 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

• 19941 clearance
• 19871 clearance
• 19861 clearance
• 19821 clearance
• 19791 clearance
• 19761 clearance

• Oxford Medilog, Inc.1 clearance
• Michael R. Kiss1 clearance
• Jackson Ent.1 clearance
• Human Technologies, Inc.1 clearance
• Farrall Instruments, Inc.1 clearance
• Behavior Research Institute, Inc.1 clearance

• K911820 — GED (GRADUATED ELECTRONIC DECELERATORBehavior Research Institute, Inc.·1994-12-05
• K871158 — SIBIS REMOTE ACTUATORHuman Technologies, Inc.·1987-05-29
• K853178 — SIBIS SELF INJURIOUS BEHAVIOR INHIBITING SYSTEMOxford Medilog, Inc.·1986-02-28
• K820622 — ELECTROSTIMULI AVERSION MACHINEMichael R. Kiss·1982-04-09
• K790738 — HABITSABATERJackson Ent.·1979-06-20
• K760166 — STIMULATOR, SONIC CONTROL (AS-1)Farrall Instruments, Inc.·1976-07-20