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 15, 2026, FDA's public records list A Plus Medical with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jan 13, 2012: BABI PLUS NEONATAL RESUSCITATION BAG.
| Jan 13, 2012 | BABI PLUS NEONATAL RESUSCITATION BAGK112852 · BTM | 510(k) clearances |
| Oct 7, 2011 | BABI PLUS INFANT NASAL CANNULA SYSTEMK110471 · BZD | 510(k) clearances |
| Aug 1, 2011 | BABI*PLUS PRESSURE RELIEF MANIFOLD - 10CM H20, 12.5CM H20, 15CM H20K110383 · BZD | 510(k) clearances |
| Nov 18, 2010 | VENTIPLUS DISPOSABLE MANOMETER 0-60 CM H2O; VENTIPLUS DISPOSABLE MANOMETER 0-20 CM H2O; VENTIPLUS DISPOSABLE MANOMETER 0K102377 · CAP | 510(k) clearances |
| May 13, 2010 | BABI PLUS INFANT NASAL CANNULA SYSTEMK093716 · BZD | 510(k) clearances |
| Nov 23, 2009 | VENTI.PLUS HYPERINFLATION BAG SYSTEM WITH PRESSURE MANOMETERK092687 · NHK | 510(k) clearances |
| May 20, 2009 | BABI*PLUS BUBBLE PAP VALVEK090317 · BYE | 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
