FDA 510(k)

PALLADIUM-103 SEED IMPLANT KITS -MULTIPLE

K-Number: K060636 · 2006-04-19

Decision Date2006-04-19

Product CodeKXK

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

PALLADIUM-103 SEED IMPLANT KITS -MULTIPLE is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2006-04-19 under 510(k) number K060636. 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 PALLADIUM-103 SEED IMPLANT KITS -MULTIPLE?

PALLADIUM-103 SEED IMPLANT KITS -MULTIPLE is a medical device that received FDA 510(k) clearance on 2006-04-19. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K060636.

When did PALLADIUM-103 SEED IMPLANT KITS -MULTIPLE receive FDA 510(k) clearance?

PALLADIUM-103 SEED IMPLANT KITS -MULTIPLE received FDA 510(k) clearance on 2006-04-19, under 510(k) number K060636.

Who is the listed applicant for PALLADIUM-103 SEED IMPLANT KITS -MULTIPLE?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PALLADIUM-103 SEED IMPLANT KITS -MULTIPLE?

The FDA product code for PALLADIUM-103 SEED IMPLANT KITS -MULTIPLE 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.