Andover Medical, Inc.
FDA 510(k) medical device clearances.
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.