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FDA 510(k)

BEBIG ISOSEED I-125

K-Number: K033781 · 2003-12-30

Decision Date2003-12-30
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BEBIG ISOSEED I-125 is the device name listed in this FDA 510(k) record. The listed applicant is Bebig Isotopen-Und Medizintechnik GmbH. It received FDA 510(k) clearance on 2003-12-30 under 510(k) number K033781. 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 BEBIG ISOSEED I-125?

BEBIG ISOSEED I-125 is a medical device that received FDA 510(k) clearance on 2003-12-30. The listed applicant is Bebig Isotopen-Und Medizintechnik GmbH. The 510(k) number is K033781.

When did BEBIG ISOSEED I-125 receive FDA 510(k) clearance?

BEBIG ISOSEED I-125 received FDA 510(k) clearance on 2003-12-30, under 510(k) number K033781.

Who is the listed applicant for BEBIG ISOSEED I-125?

The FDA 510(k) record lists Bebig Isotopen-Und Medizintechnik GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BEBIG ISOSEED I-125?

The FDA product code for BEBIG ISOSEED I-125 is KXK.

Related Clinical Trials

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.

Other records listing Bebig Isotopen-Und Medizintechnik GmbH 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.

Related Devices (Code: KXK)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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