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 Cryomedics, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jun 24, 1985: MC-4000 SURGICAL INSTRUMENTS CARDIOVASCULAR.
| Jun 24, 1985 | MC-4000 SURGICAL INSTRUMENTS CARDIOVASCULARK851152 · DWS | 510(k) clearances |
| Feb 25, 1985 | YN CO2 LASER SYSTEM 30WK844431 · HHR | 510(k) clearances |
| Jan 14, 1985 | DUAL CHANNEL TENS, PULSAR REMOTE CONTRLK842888 · GZJ | 510(k) clearances |
| Dec 7, 1984 | MC-4000 CONSOLE & PROBESK842959 · GEH | 510(k) clearances |
| Aug 1, 1984 | MT-700 MT-750 FT-350K842704 · GEH | 510(k) clearances |
| Aug 13, 1980 | KRYMED SYSTEM 4001 TILT SCOPEK801730 · HEX | 510(k) clearances |
| Apr 4, 1980 | KRYMED LIQUID NITROGEN CRYOJETK800335 · 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
