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FDA 510(k)

MICROSELECTRON - HDR FOR MOBILE ENVIRONMENT

K-Number: K925956 · 1993-11-19

ApplicantNucletron-Oldelft Corp.
Decision Date1993-11-19
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MICROSELECTRON - HDR FOR MOBILE ENVIRONMENT 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 1993-11-19 under 510(k) number K925956. 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 MICROSELECTRON - HDR FOR MOBILE ENVIRONMENT?

MICROSELECTRON - HDR FOR MOBILE ENVIRONMENT is a medical device that received FDA 510(k) clearance on 1993-11-19. The listed applicant is Nucletron-Oldelft Corp.. The 510(k) number is K925956.

When did MICROSELECTRON - HDR FOR MOBILE ENVIRONMENT receive FDA 510(k) clearance?

MICROSELECTRON - HDR FOR MOBILE ENVIRONMENT received FDA 510(k) clearance on 1993-11-19, under 510(k) number K925956.

Who is the listed applicant for MICROSELECTRON - HDR FOR MOBILE ENVIRONMENT?

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 MICROSELECTRON - HDR FOR MOBILE ENVIRONMENT?

The FDA product code for MICROSELECTRON - HDR FOR MOBILE ENVIRONMENT is JAQ.

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Other records listing Nucletron-Oldelft Corp. as applicant

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K953946MICROSELECTRON-HDR VERSION 2K953831N 800 HFK926407MODEL COLE TAB-2 TABLE W/MODEL COLE SFD-2 SPOTFILMK921991PLATO RADIATION THERAPY PLANNING SYSTEMK915622PLATO BRACHYTHERAPHY TREATMENT PLANNING SYSTEMK911612NUCLETRON 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.

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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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