FDA 510(k)

WORLDWIDE MEDICAL TECHNOLOGIES INTRACERVICAL BLOCK NEEDLE, MODEL TBD

K-Number: K982097 · 1998-06-25

ApplicantWorldwide Medical Technologies, LLC

Decision Date1998-06-25

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

WORLDWIDE MEDICAL TECHNOLOGIES INTRACERVICAL BLOCK NEEDLE, MODEL TBD 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 1998-06-25 under 510(k) number K982097. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WORLDWIDE MEDICAL TECHNOLOGIES INTRACERVICAL BLOCK NEEDLE, MODEL TBD?

WORLDWIDE MEDICAL TECHNOLOGIES INTRACERVICAL BLOCK NEEDLE, MODEL TBD is a medical device that received FDA 510(k) clearance on 1998-06-25. The listed applicant is Worldwide Medical Technologies, LLC. The 510(k) number is K982097.

When did WORLDWIDE MEDICAL TECHNOLOGIES INTRACERVICAL BLOCK NEEDLE, MODEL TBD receive FDA 510(k) clearance?

WORLDWIDE MEDICAL TECHNOLOGIES INTRACERVICAL BLOCK NEEDLE, MODEL TBD received FDA 510(k) clearance on 1998-06-25, under 510(k) number K982097.

Who is the listed applicant for WORLDWIDE MEDICAL TECHNOLOGIES INTRACERVICAL BLOCK NEEDLE, MODEL TBD?

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 INTRACERVICAL BLOCK NEEDLE, MODEL TBD?

The FDA product code for WORLDWIDE MEDICAL TECHNOLOGIES INTRACERVICAL BLOCK NEEDLE, MODEL TBD is FMI.

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Related Devices (Code: FMI)

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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.