FirmLabelled 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 Intermed with 16 510(k) clearances. The most recent is a 510(k) clearance dated May 22, 1990: NON STERILE PARENTERAL SUPPLY KIT.
| Date | Record | Source |
|---|---|---|
| May 22, 1990 | NON STERILE PARENTERAL SUPPLY KITK900857 · FMF | 510(k) clearances |
| Feb 12, 1985 | INTERMED, INS STERILE WATER/SALINEK842166 · BSY | 510(k) clearances |
| Jan 27, 1984 | DRESSING CHANGE TRAYSK833126 · | 510(k) clearances |
| Jan 11, 1984 | CENTRAL VEIN CATH. TRAY CC-20-1420K833573 · DQY | 510(k) clearances |
| Jan 11, 1984 | PERCUTANEOUS SHEATH INTRODUCER TRAYSK833574 · DQX | 510(k) clearances |
| Dec 22, 1983 | ACUTE HEMODIALYSIS TRAYSK833139 · KNZ | 510(k) clearances |
| Dec 12, 1983 | SUCTION CATHETER TRAYSK833059 · GBZ | 510(k) clearances |
| May 27, 1982 | TRACHEOSTOMY CARE TRAYSK821269 · EQN | 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
