COBE CML3— 510(k) K880021
Substantially EquivalentCobe Laboratories, Inc.
FDA 510(k) clearance K880021 for COBE CML3, Substantially Equivalent on 1988-04-01. Applicant: Cobe Laboratories, Inc.. Device class: 2.
Clearance details
- Applicant
- Cobe Laboratories, Inc.
- Product code
- Code DTZ
- Device class
- Class 2
- Regulation
- 21 CFR 870.4350
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lakewood, CO, US
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More clearances from Cobe Laboratories, Inc.
view allAdverse events under product code DTZ
product code DTZ- Death
- 182
- Injury
- 422
- Malfunction
- 3,636
- Total
- 4,240
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.