KODAK DIGITAL SCIENCE MEDICAL MODALITY ACQUISITION UNIT— 510(k) K961739
Substantially EquivalentKodak Health Imaging Systems, Inc.
FDA 510(k) clearance K961739 for KODAK DIGITAL SCIENCE MEDICAL MODALITY ACQUISITION UNIT, Substantially Equivalent on 1996-11-14. Applicant: Kodak Health Imaging Systems, Inc..
Clearance details
- Applicant
- Kodak Health Imaging Systems, Inc.
- Product code
- Code LLZ
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Dallas, TX, US
Adverse events under product code LLZ
product code LLZ- Death
- 13
- Total
- 13
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.