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 14, 2026, FDA's public records list Pymah Corp. and its 1 subsidiaries with 20 510(k) clearances. The most recent is a 510(k) clearance dated Feb 22, 1996: ATI ETHYLENE OXIDE STERILIZATION INDICATOR.
| Feb 22, 1996 | ATI ETHYLENE OXIDE STERILIZATION INDICATORK952995 · JOJ | 510(k) clearances |
| Jul 6, 1995 | ATI DISPOSABLE TEST PACK FOR STEAM STERILIZATIONK952408 · JOJ | 510(k) clearances |
| May 10, 1995 | ATI DISPOSABLE TEST PACK FOR EO GAS STERILIZATIONK951063 · JOJ | 510(k) clearances |
| Apr 18, 1995 | STERIGAGE EO 100%K934874 · JOJ | 510(k) clearances |
| Jan 27, 1995 | TRIMLINE 2000K943081 · DXN | 510(k) clearances |
| Feb 1, 1994 | ATI(R) DISP BIOLOGICAL-PLUS TEST PACKK925745 · FRC | 510(k) clearances |
| Feb 1, 1994 | ATI DISPOSABLE BIOLOGICAL-PLUS TEST PACKK925496 · FRC | 510(k) clearances |
| Nov 24, 1993 | SLIMLINE 3000K934180 · DXQ | 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
