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)

MKS BEAM OUTLINE PROJECTOR

K-Number: K921876 · 1992-06-25

ApplicantMedical Knowledge Systems, Inc.
Decision Date1992-06-25
Product CodeKPQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MKS BEAM OUTLINE PROJECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Knowledge Systems, Inc.. It received FDA 510(k) clearance on 1992-06-25 under 510(k) number K921876. 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 MKS BEAM OUTLINE PROJECTOR?

MKS BEAM OUTLINE PROJECTOR is a medical device that received FDA 510(k) clearance on 1992-06-25. The listed applicant is Medical Knowledge Systems, Inc.. The 510(k) number is K921876.

When did MKS BEAM OUTLINE PROJECTOR receive FDA 510(k) clearance?

MKS BEAM OUTLINE PROJECTOR received FDA 510(k) clearance on 1992-06-25, under 510(k) number K921876.

Who is the listed applicant for MKS BEAM OUTLINE PROJECTOR?

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

What is the FDA product code for MKS BEAM OUTLINE PROJECTOR?

The FDA product code for MKS BEAM OUTLINE PROJECTOR 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 Medical Knowledge 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.

K933493RAM-PACS

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.

↑