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FDA 510(k)

NORTHWEST RADIATION THERAPY PRODUCTS, PRECISION STEPPER AND GUIDE

K-Number: K973786 · 1998-01-02

ApplicantNw Radiation Therapy Products
Decision Date1998-01-02
Product CodeIWJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NORTHWEST RADIATION THERAPY PRODUCTS, PRECISION STEPPER AND GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Nw Radiation Therapy Products. It received FDA 510(k) clearance on 1998-01-02 under 510(k) number K973786. The device is classified under product code IWJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORTHWEST RADIATION THERAPY PRODUCTS, PRECISION STEPPER AND GUIDE?

NORTHWEST RADIATION THERAPY PRODUCTS, PRECISION STEPPER AND GUIDE is a medical device that received FDA 510(k) clearance on 1998-01-02. The listed applicant is Nw Radiation Therapy Products. The 510(k) number is K973786.

When did NORTHWEST RADIATION THERAPY PRODUCTS, PRECISION STEPPER AND GUIDE receive FDA 510(k) clearance?

NORTHWEST RADIATION THERAPY PRODUCTS, PRECISION STEPPER AND GUIDE received FDA 510(k) clearance on 1998-01-02, under 510(k) number K973786.

Who is the listed applicant for NORTHWEST RADIATION THERAPY PRODUCTS, PRECISION STEPPER AND GUIDE?

The FDA 510(k) record lists Nw Radiation Therapy Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NORTHWEST RADIATION THERAPY PRODUCTS, PRECISION STEPPER AND GUIDE?

The FDA product code for NORTHWEST RADIATION THERAPY PRODUCTS, PRECISION STEPPER AND GUIDE is IWJ.

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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Related Devices (Code: IWJ)

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.

K010166IMAGYN ISOSLEEVE / ISOSTAR NEEDLE SYSTEMImagyn Medical Technologies, Inc.K980997PGK DEVICE (MODIFIED)Pgk, Inc.K972554REGANES RADIONUCLIDE SEED MAGAZINEAvid N.I.T., Inc.K973037N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000Avid N.I.T., Inc.K974118WORLDWIDE MEDICAL TECHNOLOGIES SEED IMPLANT NEEDLE SETWorldwide Medical Technologies, LLCK973638N.I.T., INC. NEEDLE GUIDING TEMPLATEAvid N.I.T., 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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