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., part of Cook GroupLabelled 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 Cook Pacemaker Corp. with 34 510(k) clearances. The most recent is a 510(k) clearance dated May 20, 1997: LOCKING STYLET 2.
| May 20, 1997 | LOCKING STYLET 2K970690 · DQX | 510(k) clearances |
| Dec 27, 1996 | NEEDLE'S EYE SNAREK961992 · DXE | 510(k) clearances |
| Sep 29, 1995 | MINIFLEX MODEL 340, 341, AND 342 PULSE GENERATORSK953417 · DXY | 510(k) clearances |
| Sep 11, 1992 | MODEL P IN-LINE BIPOLAR ENDOCARDIAL TINED LEADK915188 · DTB | 510(k) clearances |
| Oct 16, 1991 | MODEL 340 SERIES UNIPOLAR & MODEL 5000B PROGRAMMERK905403 · DXY | 510(k) clearances |
| Oct 8, 1986 | MODEL 725TH HANDHELD TRANSCEIVER (PROGRAMMER)K863582 · DXY | 510(k) clearances |
| May 9, 1986 | SERIES (T) PROGRAMMABLE CARDIAC PULSE GENERATORSK861559 · DXY | 510(k) clearances |
| Feb 24, 1986 | MODEL 329D, SERIERS R BIOPOLAR CARDIAC PUL. GEN.K860466 · DXY | 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
