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FDA 510(k)

ISOSEED PD-103

K-Number: K993552 · 2000-03-31

ApplicantBebig Isotopentechnik GmbH
Decision Date2000-03-31
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ISOSEED PD-103 is the device name listed in this FDA 510(k) record. The listed applicant is Bebig Isotopentechnik GmbH. It received FDA 510(k) clearance on 2000-03-31 under 510(k) number K993552. 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 ISOSEED PD-103?

ISOSEED PD-103 is a medical device that received FDA 510(k) clearance on 2000-03-31. The listed applicant is Bebig Isotopentechnik GmbH. The 510(k) number is K993552.

When did ISOSEED PD-103 receive FDA 510(k) clearance?

ISOSEED PD-103 received FDA 510(k) clearance on 2000-03-31, under 510(k) number K993552.

Who is the listed applicant for ISOSEED PD-103?

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

What is the FDA product code for ISOSEED PD-103?

The FDA product code for ISOSEED PD-103 is KXK.

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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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