R. A. Fischer Co. Corp.
Mchenry, IL, US
R. A. Fischer Co. Corp. appears in FDA device records in Mchenry, IL. FDA records list 13 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 13
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 13 510(k) clearances for R. A. Fischer Co. Corp. between 1976 and 1997. The busiest year on record is 1976, with 1. The most recent is 1997, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1976 | 1 |
| 1977 | 1 |
| 1978 | 1 |
| 1980 | 1 |
| 1983 | 1 |
| 1984 | 1 |
| 1985 | 1 |
| 1987 | 1 |
| 1988 | 1 |
| 1989 | 1 |
| 1990 | 1 |
| 1996 | 1 |
| 1997 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K964208 | MD-1A GALVANIC UNIT | EGJ | Substantially Equivalent | |
| K954031 | COMPU-BLEND EPILATOR | KCW | Substantially Equivalent | |
| K895365 | MD-2 IONTOPHORESIS UNIT | EGJ | Unknown | |
| K893389 | MODEL SE-5 EPILATOR | KCW | Substantially Equivalent | |
| K884079 | MODEL CBX EPILATOR | KCW | Substantially Equivalent | |
| K871372 | CB-7 ELECTRONIC EPILATOR | KCW | Substantially Equivalent | |
| K852534 | ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9 | FTC | Substantially Equivalent | |
| K843063 | ELECTRONIC EPILATOR TS-1 | KCW | Substantially Equivalent | |
| K823674 | HIGH FREQUENCY EPILATOR CB-2 | KCW | Substantially Equivalent | |
| K801351 | EPILATOR, MODEL CP-16 | KCW | Substantially Equivalent | |
| K780076 | EPILATOR, ELECTRONIC MODEL SE-2 | KCW | Substantially Equivalent | |
| K760547 | STIMULATOR, ELECTRICAL MUSCLE (#MD-4) | IPF | Substantially Equivalent | |
| K760503 | STIMULATOR, ELECTRICAL MUSCLE (#MD-8) | IPF | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain