Acumen Medical, Inc.
Acumen Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2009.
Top product codes for Acumen Medical, Inc.
Recent clearances by Acumen Medical, Inc.
- K083855 — MODIFIED ACUMEN LEAD DELIVERY SHEATH WITH STYLET, MODEL: SPIRIT-10.5-59
- K080500 — MODIFICATION TO: ACUMEN SINGLE-LUMEN DELIVERY SHEATH, MODELS BLS-10, BLS-9, BLS-7
- K070396 — MODIFICATION TO: ACUMEN SINGLE-LUMEN DELIVERY SHEATH, MODELS BLS-8-45, BLS-7-45, BLS-6-45
- K070051 — ACUMEN INSIGHT ENDOCARDIAL VISUALIZATION SYSTEM
- K070197 — ACUMEN LEAD DELIVERY SHEATH WITH STYLET, MODELS LDS-10-64-STY AND LDS-10-57-STY
- K062145 — MODIFIED ACUMEN LEAD DELIVERY SHEATH, MODELS LDS-10-57, LDS-10-57-90, LDS-10-64 AND LDS-10-64-90
- K062084 — 7F ACUMEN CORONARY SINUS VISUALIZATION SYSTEM, MODEL CSVS-7-67
- K053400 — ACUMEN SINGLE-LUMEN DELIVERY SHEATH
- K051515 — MODIFIED ACUMEN SHEATH, MODEL TTW 10-65
- K050015 — MODIFIED ACUMEN SHEATH, MODEL TTWO767
- K042381 — CORONARY SINUS VISUALIZATION SYSTEM, MODEL CSVS5508
- K042376 — ACUMEN SHEATH, MODEL TTW7807
Data sourced from openFDA. This site is unofficial and independent of the FDA.