Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Kelowna GYN and Crook Prostate Templates

K-Number: K232949 · 2024-02-01

ApplicantVarian Medical Systems, Inc.
Decision Date2024-02-01
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Kelowna GYN and Crook Prostate Templates is a medical device manufactured by Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2024-02-01 under approval number K232949. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Kelowna GYN and Crook Prostate Templates?

Kelowna GYN and Crook Prostate Templates is a medical device that received FDA 510(k) clearance on 2024-02-01. It is manufactured by Varian Medical Systems, Inc.. The 510(k) number is K232949.

When was Kelowna GYN and Crook Prostate Templates approved by the FDA?

Kelowna GYN and Crook Prostate Templates received FDA 510(k) clearance on 2024-02-01, under approval number K232949.

What company makes Kelowna GYN and Crook Prostate Templates?

Kelowna GYN and Crook Prostate Templates is manufactured by Varian Medical Systems, Inc..

What is the FDA product code for Kelowna GYN and Crook Prostate Templates?

The FDA product code for Kelowna GYN and Crook Prostate Templates is JAQ.

Related Clinical Trials

NCT07580651 Quality and Safety of Real-Time Brachytherapy Treatments: Clinical Implementation of a Multipoint Scintillation Detector for Treatment Monitoring NOT_YET_RECRUITING

Other Devices by Varian Medical Systems, Inc.

K162476Varian High Energy Linear Accelerator K160045Heyman Packing Applicator Set K161540Advanced Breast Template System K161576Esophagus Bougie Set K160516Universal Cylinder Applicator Family, Universal Segmented Cylinder Applicator Set, Universal Stump Applicator Set, Universal Cervix Probe Set, odd lengths, Universal Cervix Probe Set, even lengths K160021Varian Sterilization Boxes

View all 83 devices →

Related Devices (Code: JAQ)

K160045Heyman Packing Applicator SetVarian Medical Systems, Inc. K161540Advanced Breast Template SystemVarian Medical Systems, Inc. K161576Esophagus Bougie SetVarian Medical Systems, Inc. K160516Universal Cylinder Applicator Family, Universal Segmented Cylinder Applicator Set, Universal Stump Applicator Set, Universal Cervix Probe Set, odd lengths, Universal Cervix Probe Set, even lengthsVarian Medical Systems, Inc. K150979CT/MR Compatible M.A.C. Interstitial GYN TemplateMick Radio-Nuclear Instruments, Inc. K160021Varian Sterilization BoxesVarian Medical Systems, Inc.

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.

↑