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FDA 510(k)

PULSED SELECTRON

K-Number: K902533 · 1990-10-12

ApplicantNucletron-Oldelft Corp.
Decision Date1990-10-12
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PULSED SELECTRON is the device name listed in this FDA 510(k) record. The listed applicant is Nucletron-Oldelft Corp.. It received FDA 510(k) clearance on 1990-10-12 under 510(k) number K902533. 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 PULSED SELECTRON?

PULSED SELECTRON is a medical device that received FDA 510(k) clearance on 1990-10-12. The listed applicant is Nucletron-Oldelft Corp.. The 510(k) number is K902533.

When did PULSED SELECTRON receive FDA 510(k) clearance?

PULSED SELECTRON received FDA 510(k) clearance on 1990-10-12, under 510(k) number K902533.

Who is the listed applicant for PULSED SELECTRON?

The FDA 510(k) record lists Nucletron-Oldelft Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PULSED SELECTRON?

The FDA product code for PULSED SELECTRON is JAQ.

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Other records listing Nucletron-Oldelft Corp. 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.

K953946MICROSELECTRON-HDR VERSION 2K953831N 800 HFK925956MICROSELECTRON - HDR FOR MOBILE ENVIRONMENTK926407MODEL COLE TAB-2 TABLE W/MODEL COLE SFD-2 SPOTFILMK921991PLATO RADIATION THERAPY PLANNING SYSTEMK915622PLATO BRACHYTHERAPHY TREATMENT PLANNING SYSTEM

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Related Devices (Code: JAQ)

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.

K262383LumenCare AzureNucletron B.V.K252717MAASTRO Rectal Applicator SetVarian Medical SystemsK251037Rectal ApplicatorNucletron B.V.K252884Guided Aarhus Applicator SetVarian Medical SystemsK250299CT/ MR Tandem and Ovoid SetVarian Medical Systems, Inc.K250289Intracavitary/Interstitial SystemVarian Medical Systems

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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