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)

POWERSERVER, POWERREADER, GATEWAY AND POWERCACHE

K-Number: K052460 · 2005-09-21

ApplicantRamsoft, Inc.
Decision Date2005-09-21
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

POWERSERVER, POWERREADER, GATEWAY AND POWERCACHE is the device name listed in this FDA 510(k) record. The listed applicant is Ramsoft, Inc.. It received FDA 510(k) clearance on 2005-09-21 under 510(k) number K052460. 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 POWERSERVER, POWERREADER, GATEWAY AND POWERCACHE?

POWERSERVER, POWERREADER, GATEWAY AND POWERCACHE is a medical device that received FDA 510(k) clearance on 2005-09-21. The listed applicant is Ramsoft, Inc.. The 510(k) number is K052460.

When did POWERSERVER, POWERREADER, GATEWAY AND POWERCACHE receive FDA 510(k) clearance?

POWERSERVER, POWERREADER, GATEWAY AND POWERCACHE received FDA 510(k) clearance on 2005-09-21, under 510(k) number K052460.

Who is the listed applicant for POWERSERVER, POWERREADER, GATEWAY AND POWERCACHE?

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

What is the FDA product code for POWERSERVER, POWERREADER, GATEWAY AND POWERCACHE?

The FDA product code for POWERSERVER, POWERREADER, GATEWAY AND POWERCACHE 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 Ramsoft, 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.

K222476OmegaAI Image ViewerK031562RAMSOFT PACS, MODEL 3.0K982563ULTRAPRO MODEL 98K942917ULTRAPRO WORKSTATION

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.

↑