SALTER LABS NEONATAL NASAL OXYGEN CANNULA— 510(k) K911740
Substantially EquivalentSalter Labs
FDA 510(k) clearance K911740 for SALTER LABS NEONATAL NASAL OXYGEN CANNULA, Substantially Equivalent on 1991-07-24. Applicant: Salter Labs. Device class: 1.
Clearance details
- Applicant
- Salter Labs
- Product code
- Code CAT
- Device class
- Class 1
- Regulation
- 21 CFR 868.5340
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Arvin, CA, US
Recent devices under product code CAT
view allMore clearances from Salter Labs
view all- K261389 — PRO2 Elite Plus Oxygen Analyzer (PRO2PLUS-1)
- K161719 — Salter Labs Bubble Humidifier
- K151874 — BiNAPS Nasal Airflow and Snore Transducer +1 more
- K151506 — Demand Nasal Oxygen Cannula, Modified Demand Nasal Oxygen Cannula
- K151421 — Nasal CO2 Sample Line, Oral Nasal CO2 Sampling Cannula, O2 Oral/Nasal Co2 Cannula, Sample Lines
Adverse events under product code CAT
product code CAT- Death
- 5
- Malfunction
- 544
- Other
- 2
- Total
- 551
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.