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 Pro-Tronics, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Apr 11, 1995: MOBIL C-ARM, REGURBISHED, VARIOUS MODELS.
| Date | Record | Source |
|---|---|---|
| Apr 11, 1995 | MOBIL C-ARM, REGURBISHED, VARIOUS MODELSK950971 · JAA | 510(k) clearances |
| Mar 14, 1995 | GENERAL ELECTRIC AMX 110, AMX II AND AMX 3K944442 · IZL | 510(k) clearances |
| Jul 2, 1990 | GENERAL ELECTRIC AMX 3K902610 · IZL | 510(k) clearances |
| May 3, 1989 | GENERAL ELECTRIC AMX 110K891143 · IZL | 510(k) clearances |
| May 1, 1989 | GENERAL ELECTRIC AMX IIK891142 · IZL | 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
