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FDA 510(k)

SELECT SEED I-125

K-Number: K002429 · 2001-02-02

ApplicantNucletron Corp.
Decision Date2001-02-02
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SELECT SEED I-125 is the device name listed in this FDA 510(k) record. The listed applicant is Nucletron Corp.. It received FDA 510(k) clearance on 2001-02-02 under 510(k) number K002429. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SELECT SEED I-125?

SELECT SEED I-125 is a medical device that received FDA 510(k) clearance on 2001-02-02. The listed applicant is Nucletron Corp.. The 510(k) number is K002429.

When did SELECT SEED I-125 receive FDA 510(k) clearance?

SELECT SEED I-125 received FDA 510(k) clearance on 2001-02-02, under 510(k) number K002429.

Who is the listed applicant for SELECT SEED I-125?

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 SELECT SEED I-125?

The FDA product code for SELECT SEED I-125 is KXK.

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Other records listing Nucletron Corp. as applicant

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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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