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FDA 510(k)

ECHOSEED/IODINE-125 SEEDS, MODEL 6733

K-Number: K010821 · 2001-04-11

ApplicantMedi-Physics Inc. Dba Nycomed Amersham Imaging
Decision Date2001-04-11
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ECHOSEED/IODINE-125 SEEDS, MODEL 6733 is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Physics Inc. Dba Nycomed Amersham Imaging. It received FDA 510(k) clearance on 2001-04-11 under 510(k) number K010821. 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 ECHOSEED/IODINE-125 SEEDS, MODEL 6733?

ECHOSEED/IODINE-125 SEEDS, MODEL 6733 is a medical device that received FDA 510(k) clearance on 2001-04-11. The listed applicant is Medi-Physics Inc. Dba Nycomed Amersham Imaging. The 510(k) number is K010821.

When did ECHOSEED/IODINE-125 SEEDS, MODEL 6733 receive FDA 510(k) clearance?

ECHOSEED/IODINE-125 SEEDS, MODEL 6733 received FDA 510(k) clearance on 2001-04-11, under 510(k) number K010821.

Who is the listed applicant for ECHOSEED/IODINE-125 SEEDS, MODEL 6733?

The FDA 510(k) record lists Medi-Physics Inc. Dba Nycomed Amersham Imaging as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ECHOSEED/IODINE-125 SEEDS, MODEL 6733?

The FDA product code for ECHOSEED/IODINE-125 SEEDS, MODEL 6733 is KXK.

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Other records listing Medi-Physics Inc. Dba Nycomed Amersham Imaging 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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