MULTIDRAW SYSTEM— 510(k) K922858
UnknownCambridge Multi-Draw, Inc.
FDA 510(k) clearance K922858 for MULTIDRAW SYSTEM, Unknown on 1992-11-16. Applicant: Cambridge Multi-Draw, Inc.. Device class: 2.
Clearance details
- Applicant
- Cambridge Multi-Draw, Inc.
- Product code
- Code GIM
- Device class
- Class 2
- Regulation
- 21 CFR 862.1675
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Cambridge, MA, US
Recent devices under product code GIM
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- K080552 — CYTO-CHEX BCT
Adverse events under product code GIM
product code GIM- Malfunction
- 1,325
- Total
- 1,325
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.