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)

CTM (CLINAC TREATMENT MONITOR)

K-Number: K770202 · 1977-02-07

ApplicantVarian Assoc., Inc.
Decision Date1977-02-07
Product CodeKPQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CTM (CLINAC TREATMENT MONITOR) is the device name listed in this FDA 510(k) record. The listed applicant is Varian Assoc., Inc.. It received FDA 510(k) clearance on 1977-02-07 under 510(k) number K770202. 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 CTM (CLINAC TREATMENT MONITOR)?

CTM (CLINAC TREATMENT MONITOR) is a medical device that received FDA 510(k) clearance on 1977-02-07. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K770202.

When did CTM (CLINAC TREATMENT MONITOR) receive FDA 510(k) clearance?

CTM (CLINAC TREATMENT MONITOR) received FDA 510(k) clearance on 1977-02-07, under 510(k) number K770202.

Who is the listed applicant for CTM (CLINAC TREATMENT MONITOR)?

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

What is the FDA product code for CTM (CLINAC TREATMENT MONITOR)?

The FDA product code for CTM (CLINAC TREATMENT MONITOR) 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 Varian Assoc., 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.

K000922PROTON VISIONK992762BRACHYVISION 6.0K992751SOMAVISIONK992753CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEMK990085MILLENNIUM MLC -120K980601VARISOURCE WRIGHT VAGINAL CUFF APPLICATOR FOR VARIAN VARISOURCE REMOTE HIGH DOSE RATE AFTERIOADER

View all 86 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.

↑