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 Andover Medical, Inc. with 21 510(k) clearances. The most recent is a 510(k) clearance dated Feb 7, 1991: CANMED 451.
| Feb 7, 1991 | CANMED 451K905729 · DRX | 510(k) clearances |
| Aug 17, 1990 | NORTECH MODEL 86901000 ELECTRODEK903427 · GXY | 510(k) clearances |
| Jan 12, 1989 | MODIFIED LABEL CHANGE TO MODEL 5455 SURGICAL CABLEK885171 · DRO | 510(k) clearances |
| May 9, 1986 | FASTRACE III, ECG ELECTRODEK860636 · DPS | 510(k) clearances |
| May 8, 1986 | ECG MONITORING/DEFIBRILLATION ELECTRODEK854433 · DRX | 510(k) clearances |
| Apr 1, 1986 | UNILATERAL OXYGEN DELIVERY SYSTEM (ULODS)K860535 · CAT | 510(k) clearances |
| Mar 31, 1986 | AMI CARDIO-PADK860283 · DRO | 510(k) clearances |
| Nov 20, 1984 | FLOW-DIRECTED PEDIATRIC THERMODIL- CATHK843410 · KRB | 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
