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FDA 510(k)

RFA A-300

K-Number: K934303 · 1994-08-09

ApplicantScanditronix, Inc.
Decision Date1994-08-09
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RFA A-300 is the device name listed in this FDA 510(k) record. The listed applicant is Scanditronix, Inc.. It received FDA 510(k) clearance on 1994-08-09 under 510(k) number K934303. 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 RFA A-300?

RFA A-300 is a medical device that received FDA 510(k) clearance on 1994-08-09. The listed applicant is Scanditronix, Inc.. The 510(k) number is K934303.

When did RFA A-300 receive FDA 510(k) clearance?

RFA A-300 received FDA 510(k) clearance on 1994-08-09, under 510(k) number K934303.

Who is the listed applicant for RFA A-300?

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

What is the FDA product code for RFA A-300?

The FDA product code for RFA A-300 is IYE.

Other records listing Scanditronix, 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.

K942092DPD-3K925133DPD-510 THERAPEUTIC RADIATION DOSIMETERK914926SCANDIPLAN - VERSION 338K904753DIOLASEK900434MM-22 MICROTRON, MM50 MICROTRONK843366SUPERPETT

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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

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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