Hudson Respiratory Care, Inc.
Hudson Respiratory Care, Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 2003.
Top product codes for Hudson Respiratory Care, Inc.
Recent clearances by Hudson Respiratory Care, Inc.
- K031383 — MODEL 780
- K011125 — NASAL CANNULA, WITH AND WITHOUT SUPPLY TUBING, AND OTHER SIMILAR NASAL CANNULA MANUFACTURED BY HRCI
- K011134 — OXYGEN SUPPLY TUBING, MODEL 1115
- K010402 — SMOOTH-FLO CIRCUIT
- K001213 — CONCHATHERM 2000 HUMIDIFICATION SYSTEM, MODELS 500-00, -10, -20, -30, -40, -50, & -60
- K993355 — HUDSON RCI CONCHA COLUMN, CAT. NO. 385-40 AND HUDSON RCI CIRCUIT, CAT. NO. 780-40, 780-41, 780-42, 780-43
- K994352 — SIDE DRAFT NEB-U-MIST NEBULIZER, MODEL 41896
- K964719 — HUDSON RCI LIFESAVER SINGLE PATIENT USE MANUAL RESUSCITATOR
- K961150 — DUAL LUMEN OXYGEN DELIVERY GAS SAMPLING CANNULA
- K961914 — BACTERIA/VIRAL FILTER
- K955645 — CATH-GUIDE
- K944301 — HUDSON RCI LIFESAVER SINGLE PATIENT USE MANUAL RESUSCITATOR CATALOG NUMBERS: 5360 THROUGH 5380
- K923946 — CONCHATHERM IV HEATED MOLECULAR HUMIDIFIER
- K930525 — MICRO MIST(TM) NEBULIZER
- K903083 — NEONATAL VENTILATOR CIRCUIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.