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FDA 510(k)

VARIPLAN COMPUT. RADIOTHERAPY

K-Number: K761265 · 1976-12-21

ApplicantVarian Assoc., Inc.
Decision Date1976-12-21
Product CodeKPQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VARIPLAN COMPUT. RADIOTHERAPY 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 1976-12-21 under 510(k) number K761265. 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 VARIPLAN COMPUT. RADIOTHERAPY?

VARIPLAN COMPUT. RADIOTHERAPY is a medical device that received FDA 510(k) clearance on 1976-12-21. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K761265.

When did VARIPLAN COMPUT. RADIOTHERAPY receive FDA 510(k) clearance?

VARIPLAN COMPUT. RADIOTHERAPY received FDA 510(k) clearance on 1976-12-21, under 510(k) number K761265.

Who is the listed applicant for VARIPLAN COMPUT. RADIOTHERAPY?

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 VARIPLAN COMPUT. RADIOTHERAPY?

The FDA product code for VARIPLAN COMPUT. RADIOTHERAPY is KPQ.

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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

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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.

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