Andover Medical, Inc.
Andover Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1991.
Top product codes for Andover Medical, Inc.
Recent clearances by Andover Medical, Inc.
- K905729 — CANMED 451
- K903427 — NORTECH MODEL 86901000 ELECTRODE
- K885171 — MODIFIED LABEL CHANGE TO MODEL 5455 SURGICAL CABLE
- K860636 — FASTRACE III, ECG ELECTRODE
- K854433 — ECG MONITORING/DEFIBRILLATION ELECTRODE
- K860535 — UNILATERAL OXYGEN DELIVERY SYSTEM (ULODS)
- K860283 — AMI CARDIO-PAD
- K843410 — FLOW-DIRECTED PEDIATRIC THERMODIL- CATH
- K843412 — FLOW DIRECTED THERMODILUTION CATH W/VEN
- K843409 — FLOW-DIRECTED THERMODILUTION CATH
- K843411 — THERMAL DILUTION CATHETER
- K831785 — NEURO EASE
- K823414 — HOLTER KIT MODEL #5000 SERIES
- K822798 — DISPOSABLE ELECTRODE #1900
- K812878 — THE NEW 1600 ELECTRODE
- K812276 — DISPOSABLE ELECTRODE, #1610
- K810271 — DIRECT CURRENT BONE GROWTH STIM. AN. PAD
- K790316 — ELECTRODE, ELECTROFLEX
- K780908 — SELF-RETAINING ELECTRODE SER. #4000-100
- K760280 — ELECTRODE SERIES 1401
- K760358 — ELECTRODE SERIES 1600
Data sourced from openFDA. This site is unofficial and independent of the FDA.