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FDA 510(k)

AVID-NIT CERVICAL REGIONAL ANESTHESIA NEEDLE

K-Number: K000117 · 2000-04-13

ApplicantAvid Medical, Inc.
Decision Date2000-04-13
Product CodeHEE
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

AVID-NIT CERVICAL REGIONAL ANESTHESIA NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Avid Medical, Inc.. It received FDA 510(k) clearance on 2000-04-13 under 510(k) number K000117. The device is classified under product code HEE. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AVID-NIT CERVICAL REGIONAL ANESTHESIA NEEDLE?

AVID-NIT CERVICAL REGIONAL ANESTHESIA NEEDLE is a medical device that received FDA 510(k) clearance on 2000-04-13. The listed applicant is Avid Medical, Inc.. The 510(k) number is K000117.

When did AVID-NIT CERVICAL REGIONAL ANESTHESIA NEEDLE receive FDA 510(k) clearance?

AVID-NIT CERVICAL REGIONAL ANESTHESIA NEEDLE received FDA 510(k) clearance on 2000-04-13, under 510(k) number K000117.

Who is the listed applicant for AVID-NIT CERVICAL REGIONAL ANESTHESIA NEEDLE?

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

What is the FDA product code for AVID-NIT CERVICAL REGIONAL ANESTHESIA NEEDLE?

The FDA product code for AVID-NIT CERVICAL REGIONAL ANESTHESIA NEEDLE is HEE.

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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Other records listing Avid Medical, 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.

K001731AVID-NIT LOSS OF RESISTANCE SYRINGE

Related Devices (Code: HEE)

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.

K052365CERVINEEDLE DISPOSABLE CARTRIDGE SYRINGERocket Medical PlcK021224ENDOCERVICAL BLOCK NEEDLEWallach Surgical Devices, Inc.K983897CERVICAL ANESTHESIA NEEDLE, CONTRACERVICAL ANESTHESIA NEEDLE, MODEL #'S 720209 30GAU X 4 MM, 720210 30GAU X 6MM, 720208GRi Mos. S.R.L.K980238GYNEX EXTENDED REACH NEEDLEGynex Corp.K973671ENDOCERVICAL BLOCK NEEDLEA & A Medical, Inc.K954718ELLMAN NEEDLE EXTENDER/MEASURED DOSE SYRINGEEllman Intl., 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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