BEBIG ISOSEED I-125
K-Number: K033781 · 2003-12-30
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Device Summary
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
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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