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FDA 510(k)

KENDALL BLUNT TUOHY EPIDURAL NEEDLE

K-Number: K954706 · 1996-05-30

ApplicantKendall Healthcare Products Co. Div.Of Tyco Health
Decision Date1996-05-30
Product CodeCAZ
Advisory CommitteeAN
DecisionUnknown

Device Summary

KENDALL BLUNT TUOHY EPIDURAL NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. It received FDA 510(k) clearance on 1996-05-30 under 510(k) number K954706. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the KENDALL BLUNT TUOHY EPIDURAL NEEDLE?

KENDALL BLUNT TUOHY EPIDURAL NEEDLE is a medical device that received FDA 510(k) clearance on 1996-05-30. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K954706.

When did KENDALL BLUNT TUOHY EPIDURAL NEEDLE receive FDA 510(k) clearance?

KENDALL BLUNT TUOHY EPIDURAL NEEDLE received FDA 510(k) clearance on 1996-05-30, under 510(k) number K954706.

Who is the listed applicant for KENDALL BLUNT TUOHY EPIDURAL NEEDLE?

The FDA 510(k) record lists Kendall Healthcare Products Co. Div.Of Tyco Health as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KENDALL BLUNT TUOHY EPIDURAL NEEDLE?

The FDA product code for KENDALL BLUNT TUOHY EPIDURAL NEEDLE is CAZ.

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Other records listing Kendall Healthcare Products Co. Div.Of Tyco Health 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.

K973763KENDALL CURITY IODOFORM PACKING STRIPK973511KENDALL CURITY PETROLATUM GAUZEK973507KENDALL XEROFORM PETROLATUM DRESSING (6311,6312,6313,6314,6315,6316,6317)K973619KENDALL CURITY NON-ADHERING DRESSINGK973509KENDALL CURASORB ZN + MG ALGINATE WOUND DRESSINGK973546KENDALL FAST-CATH PRE LUBRICATED URETHRAL CATHETER

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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.

K261372Profoject™ LOR SyringeCMT Health PTE., Ltd.K222341Arrow 0.2 Micron Flat Filter, GVSArrow International, LLCK210983BD Epilor SyringeBecton, Dickinson and CompanyK201356Plastic LOR SyringeJiangsu Caina Medical Co.,LtdK202699E-Cath STIM acc. TsuiPAJUNK GmbH MedizintechnologieK190345VPCPAJUNK GmbH Medizintechnologie

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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