Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Cryomedical Sciences with 10 510(k) clearances. The most recent is a 510(k) clearance dated Aug 22, 2001: CRYOPLAN SYSTEM.
| Date | Record | Source |
|---|---|---|
| Aug 22, 2001 | CRYOPLAN SYSTEMK011073 · GEH | 510(k) clearances |
| Sep 8, 1998 | ACCUPROBE 800 SERIES MODEL NUMBERS : 810, 820, 830, 840, 850, 860, 870 AND 880K982055 · GEH | 510(k) clearances |
| Jul 17, 1998 | CMS BLIZZARD 700 SERIES MODELS 730, 740,750,760,770,780 & 790K980668 · GEH | 510(k) clearances |
| Jul 17, 1998 | CMS BLIZZARD 700 SERIES MODELS 710, 711, 712, 720, 721 AND 722K980670 · GEH | 510(k) clearances |
| Nov 21, 1997 | ACCUPROBE 450, ACCUPROBE 550/530 AND THE ACCUPROBE 600 SERIESK973190 · GEI | 510(k) clearances |
| Jul 7, 1997 | CMS CRYOLITEK970995 · GEH | 510(k) clearances |
| Mar 20, 1997 | CMS ACCUPROBE 610, 620, 630, 640, 650, 660, 670, 680K964336 · GEH | 510(k) clearances |
| Dec 4, 1995 | CMS ACCUPROBE 550/530K953637 · GEH | 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
