KODAK DIGITAL SCIENCE MEDICAL PRINTER INTERFACE UNIT— 510(k) K961740
Substantially EquivalentKodak Health Imaging Systems, Inc.
FDA 510(k) clearance K961740 for KODAK DIGITAL SCIENCE MEDICAL PRINTER INTERFACE UNIT, Substantially Equivalent on 1996-11-14. Applicant: Kodak Health Imaging Systems, Inc.. Device class: 2.
Clearance details
- Applicant
- Kodak Health Imaging Systems, Inc.
- Product code
- Code LLZ
- Device class
- Class 2
- Regulation
- 21 CFR 892.2050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Dallas, TX, US
Recent devices under product code LLZ
view allMore clearances from Kodak Health Imaging Systems, Inc.
view all- K961739 — KODAK DIGITAL SCIENCE MEDICAL MODALITY ACQUISITION UNIT
- K961768 — KODAK DIGITAL SCIENCE FILM DIGITIZER L7501/L7506 (WITH FILM AUTOFEEDER)
- K960981 — KODAK DIGITAL SCIENCE(KDS) MEDICAL IMAGE AND INFORMATION LIBRARY
- K951807 — KODAK EKTASCAN TRIAD LASER PRINTER SYSTEM, PHOTON LASER PRINTER
- K951948 — KODAK XLS 8600 (PS)
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.