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R. A. Fischer Co. Corp.

FDA 510(k) & PMA Approved Devices — 13 products

Total Devices13
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K964208 MD-1A GALVANIC UNITEGJ1997-04-30 View
510(k) K954031 COMPU-BLEND EPILATORKCW1996-01-05 View
510(k) K895365 MD-2 IONTOPHORESIS UNITEGJ1990-06-26 View
510(k) K893389 MODEL SE-5 EPILATORKCW1989-06-05 View
510(k) K884079 MODEL CBX EPILATORKCW1988-10-04 View
510(k) K871372 CB-7 ELECTRONIC EPILATORKCW1987-04-28 View
510(k) K852534 ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9FTC1985-11-08 View
510(k) K843063 ELECTRONIC EPILATOR TS-1KCW1984-09-26 View
510(k) K823674 HIGH FREQUENCY EPILATOR CB-2KCW1983-01-14 View
510(k) K801351 EPILATOR, MODEL CP-16KCW1980-07-28 View
510(k) K780076 EPILATOR, ELECTRONIC MODEL SE-2KCW1978-01-24 View
510(k) K760547 STIMULATOR, ELECTRICAL MUSCLE (#MD-4)IPF1977-02-17 View
510(k) K760503 STIMULATOR, ELECTRICAL MUSCLE (#MD-8)IPF1976-09-27 View
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