R. A. Fischer Co. Corp.
R. A. Fischer Co. Corp. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1997.
Top product codes for R. A. Fischer Co. Corp.
Recent clearances by R. A. Fischer Co. Corp.
- K964208 — MD-1A GALVANIC UNIT
- K954031 — COMPU-BLEND EPILATOR
- K895365 — MD-2 IONTOPHORESIS UNIT
- K893389 — MODEL SE-5 EPILATOR
- K884079 — MODEL CBX EPILATOR
- K871372 — CB-7 ELECTRONIC EPILATOR
- K852534 — ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9
- K843063 — ELECTRONIC EPILATOR TS-1
- K823674 — HIGH FREQUENCY EPILATOR CB-2
- K801351 — EPILATOR, MODEL CP-16
- K780076 — EPILATOR, ELECTRONIC MODEL SE-2
- K760547 — STIMULATOR, ELECTRICAL MUSCLE (#MD-4)
- K760503 — STIMULATOR, ELECTRICAL MUSCLE (#MD-8)
Data sourced from openFDA. This site is unofficial and independent of the FDA.