510(k) K832250

SERVOMED BASIC BEDSIDE UNIT SMA 102- by Litton Medical Electronics — Product Code DRT

K832250 is an FDA 510(k) premarket notification submitted by Litton Medical Electronics for the device "SERVOMED BASIC BEDSIDE UNIT SMA 102-". The FDA issued a decision of Substantially Equivalent on Jun 1, 1984. The device falls under product code DRT (Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)), a Class II device regulated under 21 CFR 870.2300. Litton Medical Electronics has 37 other 510(k) clearances on record.