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FDA 510(k)

I-125 SEEDS CODE: 6702

K-Number: K915156 · 1992-01-06

ApplicantMedi-Physics Inc. Dba Nycomed Amersham Imaging
Decision Date1992-01-06
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

I-125 SEEDS CODE: 6702 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 1992-01-06 under 510(k) number K915156. 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 I-125 SEEDS CODE: 6702?

I-125 SEEDS CODE: 6702 is a medical device that received FDA 510(k) clearance on 1992-01-06. The listed applicant is Medi-Physics Inc. Dba Nycomed Amersham Imaging. The 510(k) number is K915156.

When did I-125 SEEDS CODE: 6702 receive FDA 510(k) clearance?

I-125 SEEDS CODE: 6702 received FDA 510(k) clearance on 1992-01-06, under 510(k) number K915156.

Who is the listed applicant for I-125 SEEDS CODE: 6702?

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 I-125 SEEDS CODE: 6702?

The FDA product code for I-125 SEEDS CODE: 6702 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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