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FDA 510(k)

IMPLANTERS/ADJUSTABLE/ANDERSON'S MARKERS

K-Number: K940121 · 1994-12-30

ApplicantBest Industries
Decision Date1994-12-30
Product CodeIWJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMPLANTERS/ADJUSTABLE/ANDERSON'S MARKERS is the device name listed in this FDA 510(k) record. The listed applicant is Best Industries. It received FDA 510(k) clearance on 1994-12-30 under 510(k) number K940121. 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 IMPLANTERS/ADJUSTABLE/ANDERSON'S MARKERS?

IMPLANTERS/ADJUSTABLE/ANDERSON'S MARKERS is a medical device that received FDA 510(k) clearance on 1994-12-30. The listed applicant is Best Industries. The 510(k) number is K940121.

When did IMPLANTERS/ADJUSTABLE/ANDERSON'S MARKERS receive FDA 510(k) clearance?

IMPLANTERS/ADJUSTABLE/ANDERSON'S MARKERS received FDA 510(k) clearance on 1994-12-30, under 510(k) number K940121.

Who is the listed applicant for IMPLANTERS/ADJUSTABLE/ANDERSON'S MARKERS?

The FDA 510(k) record lists Best Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPLANTERS/ADJUSTABLE/ANDERSON'S MARKERS?

The FDA product code for IMPLANTERS/ADJUSTABLE/ANDERSON'S MARKERS is IWJ.

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Other records listing Best Industries 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.

K933410IMPLANT APPLICATORS, CARTRIDGES/MAGAZINES, IMPLANTERS FOR PERMANENT IMPLANT OF RADIOACTIVE SEEDS/SOURCESK940119ROYAL MARSDEN GOLD GRAIN GUNK932242RADIOACTIVE SAMARIUM 145 SEEDS/SOURCES #2341-2345K924261RADIOACTIVE CESIUM-131 SEEDS/SOURCESK924290BEST INDUSTRIES CARTRIDGE & GUNK930570RADIOACTIVE PALLADIUM 103 SEEDS/SOURCES

View all 9 devices →

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, LLCK973786NORTHWEST RADIATION THERAPY PRODUCTS, PRECISION STEPPER AND GUIDENw Radiation Therapy Products

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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