CURBELL PATIENT MONITORING CABLES— 510(k) K081762
Substantially EquivalentCurbell Electronics, Inc.
FDA 510(k) clearance K081762 for CURBELL PATIENT MONITORING CABLES, Substantially Equivalent on 2008-08-27. Applicant: Curbell Electronics, Inc.. Device class: 2.
Clearance details
- Applicant
- Curbell Electronics, Inc.
- Product code
- Code DSA
- Device class
- Class 2
- Regulation
- 21 CFR 870.2900
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Greenwood Village, CO, US
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More clearances from Curbell Electronics, Inc.
view allAdverse events under product code DSA
product code DSA- Death
- 2
- Total
- 2
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.