FirmLabelled 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., part of CorningLabelled 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 Mediatech, Inc. with 24 510(k) clearances. The most recent is a 510(k) clearance dated Mar 3, 1986: CELLGRO HEPES BUFFER SOLUTION.
| Mar 3, 1986 | CELLGRO HEPES BUFFER SOLUTIONK860623 · KIT | 510(k) clearances |
| Dec 6, 1985 | PENICILLIN/STREPTOMYCIN SOLUTIONK854567 · KIT | 510(k) clearances |
| Jul 12, 1985 | CELLGRO(ISCOVE'S MEDIUM) MODIFICATIONK852485 · KIT | 510(k) clearances |
| Jul 12, 1985 | CELLGRO WILLIAMS' MEDIUM EK852475 · KIT | 510(k) clearances |
| Jul 12, 1985 | MCCOY'S 5A MEDIUM-LIQUID FORMK852602 · KIT | 510(k) clearances |
| Jul 12, 1985 | MCCOY'S 5A MEDIUM - POWDERED FORMK852603 · | 510(k) clearances |
| Jun 4, 1985 | CELLGROK852288 · KIT | 510(k) clearances |
| Mar 4, 1985 | EMEM W/NEAA-MINIMUM ESSENTIAL MED. W/NON-ESS. AMINK850510 · KIT | 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
