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FDA 510(k)

INTERSOURCE

K-Number: K973328 · 1998-12-10

ApplicantInternational Brachytherapy S.A.
Decision Date1998-12-10
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INTERSOURCE is the device name listed in this FDA 510(k) record. The listed applicant is International Brachytherapy S.A.. It received FDA 510(k) clearance on 1998-12-10 under 510(k) number K973328. 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 INTERSOURCE?

INTERSOURCE is a medical device that received FDA 510(k) clearance on 1998-12-10. The listed applicant is International Brachytherapy S.A.. The 510(k) number is K973328.

When did INTERSOURCE receive FDA 510(k) clearance?

INTERSOURCE received FDA 510(k) clearance on 1998-12-10, under 510(k) number K973328.

Who is the listed applicant for INTERSOURCE?

The FDA 510(k) record lists International Brachytherapy S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERSOURCE?

The FDA product code for INTERSOURCE is KXK.

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 International Brachytherapy S.A. 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.

K040766OPTISOURCE, MODEL 1032P

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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