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 14, 2026, FDA's public records list Life Design Systems, Inc. with 29 510(k) clearances. The most recent is a 510(k) clearance dated Dec 1, 1992: MODIFICATION MANUAL PULMON RESUSCITOR/PULMANEX(TM).
| Dec 1, 1992 | MODIFICATION MANUAL PULMON RESUSCITOR/PULMANEX(TM)K913714 · BTM | 510(k) clearances |
| Oct 11, 1989 | HUMIDI-FLEX TMK885313 · BYD | 510(k) clearances |
| Sep 18, 1989 | CHILD SIZE - FILTER FLEX (TM)K893030 · CAH | 510(k) clearances |
| May 25, 1989 | FLEX-CUP PERCUSSORK892862 · BYI | 510(k) clearances |
| May 18, 1989 | PULMONARY RESUSCITATOR, MODIFICATIONK892221 · BTM | 510(k) clearances |
| Mar 20, 1989 | OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBINGK890011 · BZO | 510(k) clearances |
| Jan 24, 1989 | MODIFIED CUSHION-FLEX(TM)K890108 · BSJ | 510(k) clearances |
| Nov 17, 1988 | CUSHION FLEX(TM)K884387 · BSJ | 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
