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FDA 510(k)

NORTH AMERICAN SCIENTIFIC (NASI) 1-125 RADIONUCLIDE BRACHYTHERAPY SOURCE

K-Number: K964647 · 1997-02-10

ApplicantNorth American Scientific, Inc.
Decision Date1997-02-10
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NORTH AMERICAN SCIENTIFIC (NASI) 1-125 RADIONUCLIDE BRACHYTHERAPY SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is North American Scientific, Inc.. It received FDA 510(k) clearance on 1997-02-10 under 510(k) number K964647. 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 NORTH AMERICAN SCIENTIFIC (NASI) 1-125 RADIONUCLIDE BRACHYTHERAPY SOURCE?

NORTH AMERICAN SCIENTIFIC (NASI) 1-125 RADIONUCLIDE BRACHYTHERAPY SOURCE is a medical device that received FDA 510(k) clearance on 1997-02-10. The listed applicant is North American Scientific, Inc.. The 510(k) number is K964647.

When did NORTH AMERICAN SCIENTIFIC (NASI) 1-125 RADIONUCLIDE BRACHYTHERAPY SOURCE receive FDA 510(k) clearance?

NORTH AMERICAN SCIENTIFIC (NASI) 1-125 RADIONUCLIDE BRACHYTHERAPY SOURCE received FDA 510(k) clearance on 1997-02-10, under 510(k) number K964647.

Who is the listed applicant for NORTH AMERICAN SCIENTIFIC (NASI) 1-125 RADIONUCLIDE BRACHYTHERAPY SOURCE?

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

What is the FDA product code for NORTH AMERICAN SCIENTIFIC (NASI) 1-125 RADIONUCLIDE BRACHYTHERAPY SOURCE?

The FDA product code for NORTH AMERICAN SCIENTIFIC (NASI) 1-125 RADIONUCLIDE BRACHYTHERAPY SOURCE is KXK.

Related Clinical Trials

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Other records listing North American Scientific, 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.

K062241ADJUSTABLE MULTI-CATHETER SOURCE APPLICTORK060679SURTRAK IMPLANTATION KITK052024NSTRAND IMPLANTATION KIT

Related Devices (Code: KXK)

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.

K252296OncoPatchOncopatch, Inc.K242818IsoSphereIsoaid, LLCK223465RadianceTx Radionuclide Brachytherapy SourceRadiance Therapeutics, Inc.K221539GammaTileGt Medical TechnologiesK202267Sirius MRI Markers, Cs-131 Preloaded Strands with Sirius MRI Markers in 18 Gauge NeedlesIsoray Medical, Inc.K193602LV Liberty Vision Model 1 90Yttrium Brachytherapy SourceLv Liberty Vision Corporation

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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