R. A. Fischer Co. Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 13
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K964208 | MD-1A GALVANIC UNIT | April 30, 1997 |
| K954031 | COMPU-BLEND EPILATOR | January 5, 1996 |
| K895365 | MD-2 IONTOPHORESIS UNIT | June 26, 1990 |
| K893389 | MODEL SE-5 EPILATOR | June 5, 1989 |
| K884079 | MODEL CBX EPILATOR | October 4, 1988 |
| K871372 | CB-7 ELECTRONIC EPILATOR | April 28, 1987 |
| K852534 | ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9 | November 8, 1985 |
| K843063 | ELECTRONIC EPILATOR TS-1 | September 26, 1984 |
| K823674 | HIGH FREQUENCY EPILATOR CB-2 | January 14, 1983 |
| K801351 | EPILATOR, MODEL CP-16 | July 28, 1980 |
| K780076 | EPILATOR, ELECTRONIC MODEL SE-2 | January 24, 1978 |
| K760547 | STIMULATOR, ELECTRICAL MUSCLE (#MD-4) | February 17, 1977 |
| K760503 | STIMULATOR, ELECTRICAL MUSCLE (#MD-8) | September 27, 1976 |