510(k) K780076

EPILATOR, ELECTRONIC MODEL SE-2 by R. A. Fischer Co. Corp. — Product Code KCW

K780076 is an FDA 510(k) premarket notification submitted by R. A. Fischer Co. Corp. for the device "EPILATOR, ELECTRONIC MODEL SE-2". The FDA issued a decision of Substantially Equivalent on Jan 24, 1978. The device falls under product code KCW (Epilator, High Frequency, Needle-Type), a Class I device regulated under 21 CFR 878.5350. R. A. Fischer Co. Corp. has 12 other 510(k) clearances on record.