FUKUDA DENSHI MODEL HC-300 END TIDAL CO2 MODULE— 510(k) K950044
Substantially EquivalentFukuda Denshi USA, Inc.
FDA 510(k) clearance K950044 for FUKUDA DENSHI MODEL HC-300 END TIDAL CO2 MODULE, Substantially Equivalent on 1995-09-15. Applicant: Fukuda Denshi USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Fukuda Denshi USA, Inc.
- Product code
- Code CCK
- Device class
- Class 2
- Regulation
- 21 CFR 868.1400
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Redmond, WA, US
Recent devices under product code CCK
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view allAdverse events under product code CCK
product code CCK- Death
- 3
- Malfunction
- 11,428
- Total
- 11,431
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.