Medical device makerLabelled 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 13, 2026, FDA's public records list Stephen Chakoff, Inc. with 16 510(k) clearances. The most recent is a 510(k) clearance dated Nov 16, 1995: HYSTERSCOPE.
| Nov 16, 1995 | HYSTERSCOPEK940316 · HIH | 510(k) clearances |
| May 24, 1995 | SINUSCOPEK940317 · EOB | 510(k) clearances |
| May 15, 1995 | CHAKOFF ENDOSCOPY (CAMERA TELEVISION ENDOSCOPIC WITHOUT AUDIOK950753 · GCJ | 510(k) clearances |
| Mar 22, 1995 | CHAKOFF ENDOSCOPY, RIGID ENDOSCOPEK951082 · GCJ | 510(k) clearances |
| Mar 6, 1995 | CHAKOFF ENDOSCOPY (LIGHT SOURCE ENDOSCOPIC XENON ARC.)K950747 · GCJ | 510(k) clearances |
| Mar 6, 1995 | CHAKOFF ENDOSCOPY (ENDOSCOPE AND/OR ACCESSORIES)K950745 · GCJ | 510(k) clearances |
| Mar 6, 1995 | CHAKOFF ENDOSCOPY (SET LAPAROSCOPY)K950746 · GCJ | 510(k) clearances |
| Mar 6, 1995 | CHAKOFF ENDOSCOPY (FIBER OPTIC LIGHT SOURCE ROUTINE)K950748 · GCJ | 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
