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FDA 510(k)

PALLADIUM SEED MODEL 100

K-Number: K852542 · 1986-01-14

ApplicantNuclear Medicine, Inc.
Decision Date1986-01-14
Product CodeIWI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PALLADIUM SEED MODEL 100 is the device name listed in this FDA 510(k) record. The listed applicant is Nuclear Medicine, Inc.. It received FDA 510(k) clearance on 1986-01-14 under 510(k) number K852542. The device is classified under product code IWI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PALLADIUM SEED MODEL 100?

PALLADIUM SEED MODEL 100 is a medical device that received FDA 510(k) clearance on 1986-01-14. The listed applicant is Nuclear Medicine, Inc.. The 510(k) number is K852542.

When did PALLADIUM SEED MODEL 100 receive FDA 510(k) clearance?

PALLADIUM SEED MODEL 100 received FDA 510(k) clearance on 1986-01-14, under 510(k) number K852542.

Who is the listed applicant for PALLADIUM SEED MODEL 100?

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

What is the FDA product code for PALLADIUM SEED MODEL 100?

The FDA product code for PALLADIUM SEED MODEL 100 is IWI.

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Related Devices (Code: IWI)

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.

K973363NORTH AMERICAN SCIENTIFIC(NASI)PD-103 RADIONUCLIDE BRACHYTHERAPY SOURCE-MODEL MED3633Ml Strategies, Inc.K940632I-125 RAPID STRANDMedi-Physics Inc. Dba Nycomed Amersham ImagingK912170RADIOACTIVE IODINE-125 SOURCESBest IndustriesK882449CESIUM 137 SOURCE, MODEL CSM-40Cis-Us, Inc.K874787MODIFIED PALLADIUM SEED MODEL 100Theragenics Corp.

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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