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 Panmed, Inc. with 16 510(k) clearances. The most recent is a 510(k) clearance dated Nov 13, 1986: ERYTHOCYTE CREATINE.
| Date | Record | Source |
|---|---|---|
| Nov 13, 1986 | ERYTHOCYTE CREATINEK852767 · JLA | 510(k) clearances |
| Apr 14, 1982 | SICKLE-CHECKK820642 · GHM | 510(k) clearances |
| Oct 10, 1980 | AMMONIUM MOLYBDATE INORGANIC PHOSPHORUSK802159 · CEO | 510(k) clearances |
| Oct 10, 1980 | POSTASSIUM BUFFER SOL. & WASH SOLUTIONK802158 · CEM | 510(k) clearances |
| Oct 10, 1980 | REAGENTS SERUM CREATINE USING TECHICONK802156 · CGX | 510(k) clearances |
| Oct 10, 1980 | BIURET REAGENT & TOTAL PROTEIN BLANK SOLK802161 · CEK | 510(k) clearances |
| Oct 10, 1980 | BUN COLOR REAGENT & BUN ACID USEDK802160 · CDW | 510(k) clearances |
| Oct 10, 1980 | REAGENTS SERUM SODIUM USING THE TECH.K802155 · JGS | 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
