Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list E.M. Adams Co. with 23 510(k) clearances. The most recent is a 510(k) clearance dated Aug 6, 1997: PATIENT RESTRAINT.
| Aug 6, 1997 | PATIENT RESTRAINTK971948 · FMQ | 510(k) clearances |
| Jul 1, 1997 | RESTRAINTS (VESTS AND JACKETS)K971536 · FMQ | 510(k) clearances |
| Apr 25, 1991 | SPLASH GUARDK905173 · KYZ | 510(k) clearances |
| Mar 21, 1991 | STERILE DISPOSABLE DRAPE(S)K910468 · FZI | 510(k) clearances |
| Nov 23, 1987 | DISPOSABLE BIPOLAR FORCEPSK873978 · GEN | 510(k) clearances |
| Feb 21, 1985 | INSTRUMENT POCKETK850063 · | 510(k) clearances |
| Jan 10, 1985 | I.V. START KIT & OBSTETRICAL KITK843724 · KKX | 510(k) clearances |
| Dec 19, 1984 | WET PACKK843783 · EFQ | 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
