Catheter Connections, Inc.
Catheter Connections, Inc. holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2015, with 1 FDA device recall on record.
Top product codes for Catheter Connections, Inc.
FDA recalls by Catheter Connections, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Catheter Connections, Inc.
- K142806 — DualCap
- K142399 — DualCap IV Pole Strips(Disinfectant Caps for Male Luers)
- K123967 — CATHETER CONNECTIONS' DARK BLUE DUALCAP FOR MALE LUERS
- K123065 — CATHETER CONNECTIONS DUALCAP SOLO
- K113842 — CATHETER CONNECTIONS' DUALCAP SOLO
- K112985 — CATHETER CONNECTIONS' DUALCAP DUO
- K093229 — CATHETER CONNECTIONS DUALCAP
Data sourced from openFDA. This site is unofficial and independent of the FDA.