Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

KODAK DIGITAL SCIENCE MEDICAL MODALITY ACQUISITION UNIT

K-Number: K961739 · 1996-11-14

ApplicantKodak Health Imaging Systems, Inc.
Decision Date1996-11-14
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK DIGITAL SCIENCE MEDICAL MODALITY ACQUISITION UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Kodak Health Imaging Systems, Inc.. It received FDA 510(k) clearance on 1996-11-14 under 510(k) number K961739. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK DIGITAL SCIENCE MEDICAL MODALITY ACQUISITION UNIT?

KODAK DIGITAL SCIENCE MEDICAL MODALITY ACQUISITION UNIT is a medical device that received FDA 510(k) clearance on 1996-11-14. The listed applicant is Kodak Health Imaging Systems, Inc.. The 510(k) number is K961739.

When did KODAK DIGITAL SCIENCE MEDICAL MODALITY ACQUISITION UNIT receive FDA 510(k) clearance?

KODAK DIGITAL SCIENCE MEDICAL MODALITY ACQUISITION UNIT received FDA 510(k) clearance on 1996-11-14, under 510(k) number K961739.

Who is the listed applicant for KODAK DIGITAL SCIENCE MEDICAL MODALITY ACQUISITION UNIT?

The FDA 510(k) record lists Kodak Health Imaging Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KODAK DIGITAL SCIENCE MEDICAL MODALITY ACQUISITION UNIT?

The FDA product code for KODAK DIGITAL SCIENCE MEDICAL MODALITY ACQUISITION UNIT is LLZ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Kodak Health Imaging Systems, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K961740KODAK DIGITAL SCIENCE MEDICAL PRINTER INTERFACE UNITK961768KODAK DIGITAL SCIENCE FILM DIGITIZER L7501/L7506 (WITH FILM AUTOFEEDER)K960981KODAK DIGITAL SCIENCE(KDS) MEDICAL IMAGE AND INFORMATION LIBRARYK951948KODAK XLS 8600 (PS)K951807KODAK EKTASCAN TRIAD LASER PRINTER SYSTEM, PHOTON LASER PRINTER

Related Devices (Code: LLZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261874Syneris PACS v.1.0.1.0SynerisK262442HipStudio AnalysisReplasia BVK261855Elucid PlaqueIQElucid Bioimaging, Inc.K254214OOOPDSTaiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑