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FDA 510(k)

GOLD SEADS

K-Number: K834027 · 1983-12-27

ApplicantRadiation Safety & Nuclear Products, Inc.
Decision Date1983-12-27
Product CodeIWG
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GOLD SEADS is the device name listed in this FDA 510(k) record. The listed applicant is Radiation Safety & Nuclear Products, Inc.. It received FDA 510(k) clearance on 1983-12-27 under 510(k) number K834027. The device is classified under product code IWG. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GOLD SEADS?

GOLD SEADS is a medical device that received FDA 510(k) clearance on 1983-12-27. The listed applicant is Radiation Safety & Nuclear Products, Inc.. The 510(k) number is K834027.

When did GOLD SEADS receive FDA 510(k) clearance?

GOLD SEADS received FDA 510(k) clearance on 1983-12-27, under 510(k) number K834027.

Who is the listed applicant for GOLD SEADS?

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

What is the FDA product code for GOLD SEADS?

The FDA product code for GOLD SEADS is IWG.

Related Clinical Trials

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.

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Other records listing Radiation Safety & Nuclear Products, Inc. as applicant

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.

K850382IRIDIUM SEEDS

Related Devices (Code: IWG)

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.

K081066BRACHYTHERAPY SOURCE DEVICE, MODEL 9011Medi-Physics, Inc., Dba GE HealthcareK982421IMAGYN 125 I SEED, MODEL IS 125International Isotopes, Inc.

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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