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FDA 510(k)

ADVANCED THERAPY DOSIMETER

K-Number: K942083 · 1994-09-02

ApplicantKeithley Instruments, Inc.
Decision Date1994-09-02
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ADVANCED THERAPY DOSIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Keithley Instruments, Inc.. It received FDA 510(k) clearance on 1994-09-02 under 510(k) number K942083. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANCED THERAPY DOSIMETER?

ADVANCED THERAPY DOSIMETER is a medical device that received FDA 510(k) clearance on 1994-09-02. The listed applicant is Keithley Instruments, Inc.. The 510(k) number is K942083.

When did ADVANCED THERAPY DOSIMETER receive FDA 510(k) clearance?

ADVANCED THERAPY DOSIMETER received FDA 510(k) clearance on 1994-09-02, under 510(k) number K942083.

Who is the listed applicant for ADVANCED THERAPY DOSIMETER?

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

What is the FDA product code for ADVANCED THERAPY DOSIMETER?

The FDA product code for ADVANCED THERAPY DOSIMETER is IYE.

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 Keithley Instruments, 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.

K932598TN-RD-50K874893MODEL 35300 TRACKER(TM) THERAPY BEAM EVALUATORK854110KEITHLEY MODEL 75100 & 75200

Related Devices (Code: IYE)

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.

K261865AerFrame™ Alignment Laser Box (LBV2)Stabilix, LLCK261718EZFluence (RADEZ V2)Radformation, Inc.K260733MRIA Radiation Therapy Information System (MRIA)Manteia Technologies Co., Ltd.K261856Halcyon, Ethos Radiotherapy System (5.0)Varian Medical Systems, Inc.K252937ThinkQA 3Dosisoft SAK253004LUNA 3DLap GmbH Laser Applikationen

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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