510(k) K935351

A.C. POWER PATIENT LIFT by Ken Kemmerer — Product Code FNG

K935351 is an FDA 510(k) premarket notification submitted by Ken Kemmerer for the device "A.C. POWER PATIENT LIFT". The FDA issued a decision of Substantially Equivalent on February 28, 1994. The device falls under product code FNG (Lift, Patient, Ac-Powered), a Class II device regulated under 21 CFR 880.5500. Ken Kemmerer has at least 1 other 510(k) clearance on record.