510(k) K940130

STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER by Stryker Corp. — Product Code FPP

K940130 is an FDA 510(k) premarket notification submitted by Stryker Corp. for the device "STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER". The FDA issued a decision of Substantially Equivalent on March 10, 1994. The device falls under product code FPP (Stretcher, Hand-Carried), a Class I device regulated under 21 CFR 880.6900. Stryker Corp. has at least 10 other 510(k) clearances on record.