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)

RADIATION BEAM DATA ACQUISTIOIN SYSTEMS

K-Number: K854880 · 1986-01-10

ApplicantComputerized Medical Systems, Inc.
Decision Date1986-01-10
Product CodeKPQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADIATION BEAM DATA ACQUISTIOIN SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Computerized Medical Systems, Inc.. It received FDA 510(k) clearance on 1986-01-10 under 510(k) number K854880. The device is classified under product code KPQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIATION BEAM DATA ACQUISTIOIN SYSTEMS?

RADIATION BEAM DATA ACQUISTIOIN SYSTEMS is a medical device that received FDA 510(k) clearance on 1986-01-10. The listed applicant is Computerized Medical Systems, Inc.. The 510(k) number is K854880.

When did RADIATION BEAM DATA ACQUISTIOIN SYSTEMS receive FDA 510(k) clearance?

RADIATION BEAM DATA ACQUISTIOIN SYSTEMS received FDA 510(k) clearance on 1986-01-10, under 510(k) number K854880.

Who is the listed applicant for RADIATION BEAM DATA ACQUISTIOIN SYSTEMS?

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

What is the FDA product code for RADIATION BEAM DATA ACQUISTIOIN SYSTEMS?

The FDA product code for RADIATION BEAM DATA ACQUISTIOIN SYSTEMS is KPQ.

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 Computerized Medical 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.

K110730MONACO RTP SYSTEMK102216XIO RTP SYSTEMK092132XIO RTP SYSTEMK091179MONACO RTP SYSTEM, VMAT OPTIONK080799ATLAS-BASED AUTOSEGMENTATIONK071938MONACO RTP SYSTEM

View all 23 devices →

Related Devices (Code: KPQ)

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.

K132045ADVANTAGESIM MD WITH CT ATLAS-BASED CONTOURING AND RE-PLANNING OPTIONSGe Hungary KftK101038RAD II SIMULATOR, RAD II KV IMAGER, DUAL RAD II KV IMAGERAcceletronics Digital Imaging, LLCK090706ONCENTRA SIMULATION 2.3Nucletron CorporationK083591IKOENGELO, VERSION 2Ikoetech, LLCK072445INTEGRATED BRACHYTHERAPY UNIT - DIGITALNucletron Corp.K061006IKOENGELOIkoetech, 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.

↑