R. A. Fischer Co. Corp.
FDA 510(k) medical device clearances.
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.