Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Medtronic Andover Medical, Inc.

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K910494 RESTING EKG ELECTRODE SERIESDRX1991-04-22 View
510(k) K905446 MEDITRONIC ANDOVER MEDICAL MODEL 1690 ELECTRODEDRX1991-02-05 View
510(k) K903018 MEDTRONIC ANDOVER MEDICAL SAF-D-FIB MODEL 1220-002LDD1990-12-03 View
510(k) K903554 NORTECH MODEL 87202204 ELECTRODEGXY1990-08-30 View
510(k) K882174 MODIFIED MODEL 5455 DISPOSABLE SURGICAL CABLEDSA1988-07-22 View
510(k) K852469 SAF-D-FIBDRX1985-09-16 View
↑