Life Design Systems, Inc.
Life Design Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1982, most recent 1992.
Top product codes for Life Design Systems, Inc.
Recent clearances by Life Design Systems, Inc.
- K913714 — MODIFICATION MANUAL PULMON RESUSCITOR/PULMANEX(TM)
- K885313 — HUMIDI-FLEX TM
- K893030 — CHILD SIZE - FILTER FLEX (TM)
- K892862 — FLEX-CUP PERCUSSOR
- K892221 — PULMONARY RESUSCITATOR, MODIFICATION
- K890011 — OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBING
- K890108 — MODIFIED CUSHION-FLEX(TM)
- K884387 — CUSHION FLEX(TM)
- K884068 — PULMANEX TM (NEO-NATAL SIZE)
- K873179 — HEATER WIRE BREATHING CIRCUIT
- K863857 — PULSE-OX
- K864681 — CARHILL ONE-WAY RESUSCITATION VALVE
- K871669 — BABYSET(TM) MODIFIED JACKSON-REES CIRCUIT W/VALVE
- K862448 — FLOW GENERATOR FOR SLEEP APNEA, LDS 1500
- K863026 — PULMANEX TM (MODIFICATION)
- K861758 — CUSHION-FLEX TM NASAL CPAP MASK FOR SLEEP APNEA
- K860659 — END TIDAL CO2 SAMPLING CIRCUIT
- K860693 — PULMANEX (TM)
- K854822 — LDS PEEP VALVE
- K854458 — CUSHION-FLEX TM-CPAP FACE MASK
- K854537 — HEADSTRAP
- K854037 — PULMANEX
- K844729 — RESUSCITATOR, PULMONARY, MANUAL
- K843169 — CUSHION-FLEX TM
- K841264 — BABYSET TM & PAC TM -PULMONARY ASSIST
- K841236 — FILTER-FLEX
- K822116 — ANESTHESIA BREATHING BAG, VARIOUS SIZES
- K821846 — LDS MONITORING ELECTRODE
- K821087 — ANESTHESIA BREATHING CIRCUIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.