Catheter Research, Inc.
Catheter Research, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2013, with 1 FDA device recall on record.
Top product codes for Catheter Research, Inc.
FDA recalls by Catheter Research, 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 Research, Inc.
- K123258 — THE ADVANCE CATHETER FOR HSG AND SIS
- K120154 — INTRAUTERINE INSEMINATION (IUI) CATHETER
- K032835 — H/S CATHETER SET
- K020292 — UTERINE INJECTOR
- K973839 — DISPOSABLE ESOPHAGEAL STETHOSCOPE
- K974357 — UTERINE MANIPULATOR/INJECTOR
- K951345 — DISPOSABLE AIRWAY CONNECTORS FOR GAS SAMPLING
- K946044 — DISPOSABLE GAS SAMPLING LINES
Data sourced from openFDA. This site is unofficial and independent of the FDA.