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)

ADVIEWER 2000

K-Number: K952188 · 1995-05-30

ApplicantAdp , Ltd.
Decision Date1995-05-30
Product CodeIXC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADVIEWER 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Adp , Ltd.. It received FDA 510(k) clearance on 1995-05-30 under 510(k) number K952188. The device is classified under product code IXC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVIEWER 2000?

ADVIEWER 2000 is a medical device that received FDA 510(k) clearance on 1995-05-30. The listed applicant is Adp , Ltd.. The 510(k) number is K952188.

When did ADVIEWER 2000 receive FDA 510(k) clearance?

ADVIEWER 2000 received FDA 510(k) clearance on 1995-05-30, under 510(k) number K952188.

Who is the listed applicant for ADVIEWER 2000?

The FDA 510(k) record lists Adp , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ADVIEWER 2000?

The FDA product code for ADVIEWER 2000 is IXC.

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

Related Devices (Code: IXC)

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.

K991302SMARTLIGHT DIGITAL FILM VIEWER, MODELS SL 4000PLUS, SL 2000PLUSSmartlight, Inc.K973965SMART MOTORIZED VIEWERSmartlight, Ltd.K973115ARRIPRO 35 ST/TVArnold & Richter Cine TechnikK970240DIFFUSER PANELFocused Viewer, Inc.K954998LILY DARK VIEWERLily Imaging Solutions Co.K954199VOXBOXVoxel

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.

↑