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 Portable Power Systems, Inc. with 18 510(k) clearances. The most recent is a 510(k) clearance dated May 2, 1997: SEALED LEAD ACID BATTERY PACK.
| May 2, 1997 | SEALED LEAD ACID BATTERY PACKK970234 · IZL | 510(k) clearances |
| Aug 2, 1995 | PHYSIO CONTROL LIFEPAK 200 AUTO DEFIBRILLATORK946080 · FCO | 510(k) clearances |
| Jan 20, 1995 | BATTERY PACK #PMX120-18AK945043 · IZL | 510(k) clearances |
| Feb 17, 1994 | REPLACEMENT BATERY FOR GE AMX-4 PORT. X-RAY MACH.K931483 · IZL | 510(k) clearances |
| Feb 17, 1994 | BATTERY PACK# S1009LAK933065 · DPS | 510(k) clearances |
| Feb 17, 1994 | BATTERY PACK# S1024NCK934508 · LDD | 510(k) clearances |
| Feb 17, 1994 | BATTERY PACK# S1018LA FOR IVAC 4000, 4200 VITAL CHECKK932823 · DXN | 510(k) clearances |
| Feb 17, 1994 | REPLACEMENT BATTER FOR ABBOTT LABS LIFECARE 4100 SK931484 · BZD | 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
