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FDA 510(k)

WORLDWIDE MEDICAL TECHNOLOGIES NEEDLE GUIDE

K-Number: K981470 · 1998-06-19

ApplicantWorldwide Medical Technologies, LLC
Decision Date1998-06-19
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

WORLDWIDE MEDICAL TECHNOLOGIES NEEDLE GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Worldwide Medical Technologies, LLC. It received FDA 510(k) clearance on 1998-06-19 under 510(k) number K981470. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WORLDWIDE MEDICAL TECHNOLOGIES NEEDLE GUIDE?

WORLDWIDE MEDICAL TECHNOLOGIES NEEDLE GUIDE is a medical device that received FDA 510(k) clearance on 1998-06-19. The listed applicant is Worldwide Medical Technologies, LLC. The 510(k) number is K981470.

When did WORLDWIDE MEDICAL TECHNOLOGIES NEEDLE GUIDE receive FDA 510(k) clearance?

WORLDWIDE MEDICAL TECHNOLOGIES NEEDLE GUIDE received FDA 510(k) clearance on 1998-06-19, under 510(k) number K981470.

Who is the listed applicant for WORLDWIDE MEDICAL TECHNOLOGIES NEEDLE GUIDE?

The FDA 510(k) record lists Worldwide Medical Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WORLDWIDE MEDICAL TECHNOLOGIES NEEDLE GUIDE?

The FDA product code for WORLDWIDE MEDICAL TECHNOLOGIES NEEDLE GUIDE is IZH.

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Other records listing Worldwide Medical Technologies, LLC 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.

K062214BRACHYSCIENCES STRANDPORTK023179READI-STRAND, MODEL PSSTRANDK022705READI-STRAND, MODEL PSSTRANDK022389READI-LOAD SYSTEM, MODEL PSS 1820RLK020641SPIRITUS(TM) RESPIRATORY SYSTEM #SRS 001K020337READI-STRAND; MODEL PSSTRAND

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Related Devices (Code: IZH)

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.

K203509SMART FINDERIms Giotto S.P.A.K202294Affirm Contrast BiopsyHologic, Inc.K191495Biopsy PositionerFujifilm CorporationK161575Affirm Lateral Arm Upright Biopsy AccessoryHologicK161920Comfort CoverPrecision Dynamics CorporationK153486Affirm Prone Biopsy SystemHologic, Inc.

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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