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FDA 510(k)

SEED SELECTRON MODEL V. 1.0

K-Number: K010032 · 2001-10-17

ApplicantNucletron Corp.
Decision Date2001-10-17
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SEED SELECTRON MODEL V. 1.0 is the device name listed in this FDA 510(k) record. The listed applicant is Nucletron Corp.. It received FDA 510(k) clearance on 2001-10-17 under 510(k) number K010032. 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 SEED SELECTRON MODEL V. 1.0?

SEED SELECTRON MODEL V. 1.0 is a medical device that received FDA 510(k) clearance on 2001-10-17. The listed applicant is Nucletron Corp.. The 510(k) number is K010032.

When did SEED SELECTRON MODEL V. 1.0 receive FDA 510(k) clearance?

SEED SELECTRON MODEL V. 1.0 received FDA 510(k) clearance on 2001-10-17, under 510(k) number K010032.

Who is the listed applicant for SEED SELECTRON MODEL V. 1.0?

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

What is the FDA product code for SEED SELECTRON MODEL V. 1.0?

The FDA product code for SEED SELECTRON MODEL V. 1.0 is JAQ.

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Other records listing Nucletron 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.

K092804MICROSELECTRON HDR V2, MODEL 105.999K091598LUMENCATH APPLICATOR SET, MODELS 189. 795, 189.796, 189.797, 189.798, LUMENCATH CATHETERSK072445INTEGRATED BRACHYTHERAPY UNIT - DIGITALK041715INTRACAVITARY MOULD APPLICATOR SET, MODEL 189.001K041933MICROSELECTRON PDRK041719ONCENTRA-VISIR

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Related Devices (Code: JAQ)

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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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