Medical device makerLabelled 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.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list J. H. Emerson Co. with 25 510(k) clearances. The most recent is a 510(k) clearance dated Nov 22, 2000: EMERSON COUGH ASSIST MODEL CA-3000 W/AUTOMATIC TIMING AND MODEL CM-3000 W/MANUAL TIMING.
| Nov 22, 2000 | EMERSON COUGH ASSIST MODEL CA-3000 W/AUTOMATIC TIMING AND MODEL CM-3000 W/MANUAL TIMINGK002598 · NHJ | 510(k) clearances |
| Jan 12, 1993 | OXYGEN POWERED RESUSCITATOR FOR CPRK920910 · BTL | 510(k) clearances |
| Nov 17, 1992 | EMERSON IN-EXSUFFLATOR, MODELS 2-CM & 2-CAK924174 · NHJ | 510(k) clearances |
| Nov 19, 1990 | EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARMK902764 · BYT | 510(k) clearances |
| Jan 22, 1990 | MODEL 7-AT TREATMENT CHAMBERK896721 · LGM | 510(k) clearances |
| Aug 4, 1988 | EMERSON CHEST RESPIRATOR, MODEL 33-CREK881808 · BYT | 510(k) clearances |
| Dec 29, 1987 | EMERSON DISPOS THORACIC DRAINAGE SET - 551-8000K873489 · GCX | 510(k) clearances |
| Sep 24, 1987 | 97-TD EMERSON TIMER/DIMMER CONTROLK872937 · IQA | 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
