FirmLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list R. A. Fischer Co. Corp. with 13 510(k) clearances. The most recent is a 510(k) clearance dated Apr 30, 1997: MD-1A GALVANIC UNIT.
| Apr 30, 1997 | MD-1A GALVANIC UNITK964208 · EGJ | 510(k) clearances |
| Jan 5, 1996 | COMPU-BLEND EPILATORK954031 · KCW | 510(k) clearances |
| Jun 26, 1990 | MD-2 IONTOPHORESIS UNITK895365 · EGJ | 510(k) clearances |
| Jun 5, 1989 | MODEL SE-5 EPILATORK893389 · KCW | 510(k) clearances |
| Oct 4, 1988 | MODEL CBX EPILATORK884079 · KCW | 510(k) clearances |
| Apr 28, 1987 | CB-7 ELECTRONIC EPILATORK871372 · KCW | 510(k) clearances |
| Nov 8, 1985 | ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9K852534 · FTC | 510(k) clearances |
| Sep 26, 1984 | ELECTRONIC EPILATOR TS-1K843063 · KCW | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
