R. A. Fischer Co. Corp. FDA Record
- No warning letters matched by name
R. A. Fischer Co. Corp. has 0 FDA recalls, 0 inspections, 13 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "R. A. Fischer Co. Corp." is on file.
- Latest 510(k)
- Apr 30, 1997
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 11, 2026 (checked Nov 15, 2026, unchanged) | File dated Nov 10, 2026 | Current |
| 510(k) clearances | 13 | Nov 15, 2026 | File dated Nov 9, 2026 | Current |
| Inspections | 0 | Nov 15, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
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Recent 510(k) clearances
| K-Number | Device | Date |
|---|---|---|
| K964208 | MD-1A GALVANIC UNIT | Apr 30, 1997 |
| K954031 | COMPU-BLEND EPILATOR | Jan 5, 1996 |
| K895365 | MD-2 IONTOPHORESIS UNIT | Jun 26, 1990 |
| K893389 | MODEL SE-5 EPILATOR | Jun 5, 1989 |
| K884079 | MODEL CBX EPILATOR | Oct 4, 1988 |
| K871372 | CB-7 ELECTRONIC EPILATOR | Apr 28, 1987 |
| K852534 | ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9 | Nov 8, 1985 |
| K843063 | ELECTRONIC EPILATOR TS-1 | Sep 26, 1984 |
| K823674 | HIGH FREQUENCY EPILATOR CB-2 | Jan 14, 1983 |
| K801351 | EPILATOR, MODEL CP-16 | Jul 28, 1980 |
| K780076 | EPILATOR, ELECTRONIC MODEL SE-2 | Jan 24, 1978 |
| K760547 | STIMULATOR, ELECTRICAL MUSCLE (#MD-4) | Feb 17, 1977 |
| K760503 | STIMULATOR, ELECTRICAL MUSCLE (#MD-8) | Sep 27, 1976 |
R. A. Fischer Co. Corp. and the FDA: common questions
Has R. A. Fischer Co. Corp. received an FDA warning letter?
No FDA warning letter addressed to the name "R. A. Fischer Co. Corp." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.
Has R. A. Fischer Co. Corp. received an FDA Form 483?
FDA has not published a Form 483 for "R. A. Fischer Co. Corp." in its reading room. FDA publishes some Form 483s, not all of them.
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