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FDA 510(k)

AVID-NIT NERVE STIMULATION NEEDLES

K-Number: K014246 · 2002-07-16

ApplicantAvid N.I.T., Inc.
Decision Date2002-07-16
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AVID-NIT NERVE STIMULATION NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Avid N.I.T., Inc.. It received FDA 510(k) clearance on 2002-07-16 under 510(k) number K014246. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AVID-NIT NERVE STIMULATION NEEDLES?

AVID-NIT NERVE STIMULATION NEEDLES is a medical device that received FDA 510(k) clearance on 2002-07-16. The listed applicant is Avid N.I.T., Inc.. The 510(k) number is K014246.

When did AVID-NIT NERVE STIMULATION NEEDLES receive FDA 510(k) clearance?

AVID-NIT NERVE STIMULATION NEEDLES received FDA 510(k) clearance on 2002-07-16, under 510(k) number K014246.

Who is the listed applicant for AVID-NIT NERVE STIMULATION NEEDLES?

The FDA 510(k) record lists Avid N.I.T., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AVID-NIT NERVE STIMULATION NEEDLES?

The FDA product code for AVID-NIT NERVE STIMULATION NEEDLES is CAZ.

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Other records listing Avid N.I.T., Inc. 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.

K013231AVID-NIT PLASTIC HUB LUTZ EPIDURAL NEEDLE,MODEL RP2035L, AVID-NIT METAL HUB LUTZ EPIDURAL NEEDLE, MODEL RM2035LK983218N,I.T., INC. AUTOMATIC CUTTING BIOPSY NEEDLEK972595ALDRETE EPIDURAL NEEDLE WITHOUT INTRODUCERK972554REGANES RADIONUCLIDE SEED MAGAZINEK973037N.I.T., INC. RADIONUCLIDE SEED APPLICATOR, MODEL SA-1000K973638N.I.T., INC. NEEDLE GUIDING TEMPLATE

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Related Devices (Code: CAZ)

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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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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