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 Harmac Medical Products with 8 510(k) clearances. The most recent is a 510(k) clearance dated Aug 29, 2002: HARMAC HUBER NEEDLE SAFETY DEVICE, H2984001.
| Aug 29, 2002 | HARMAC HUBER NEEDLE SAFETY DEVICE, H2984001K021916 · FPA | 510(k) clearances |
| Oct 16, 1997 | HARMAC BALLOON ANGIOGRAPHIC CATHETERK962829 · DQO | 510(k) clearances |
| Oct 16, 1997 | HARMAC BALLOON WEDGE PRESSURE CATHETERK963335 · DQO | 510(k) clearances |
| Oct 15, 1997 | HARMAC TEMPORARY PACING CATHETER WITH BALLOONK962833 · LDF | 510(k) clearances |
| Aug 14, 1997 | HARMAC THERMODILUTION CATHETERK963336 · DYG | 510(k) clearances |
| Aug 14, 1997 | HARMAC BIPOLAR TEMPORARY PACING CATHETER WITH STYLETK963073 · LDF | 510(k) clearances |
| Jun 25, 1997 | HARMAC QUADPOLAR MAPPING PACING CATHETERK963074 · DRF | 510(k) clearances |
| Sep 1, 1995 | HARMAC EXTENSION INFUSION SETK950895 · FPA | 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
