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FDA 510(k)

CURITY SPINAL ANESTHESIA TRAY

K-Number: K903761 · 1990-12-19

ApplicantKendall Healthcare Products Co. Div.Of Tyco Health
Decision Date1990-12-19
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CURITY SPINAL ANESTHESIA TRAY 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 1990-12-19 under 510(k) number K903761. 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 CURITY SPINAL ANESTHESIA TRAY?

CURITY SPINAL ANESTHESIA TRAY is a medical device that received FDA 510(k) clearance on 1990-12-19. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K903761.

When did CURITY SPINAL ANESTHESIA TRAY receive FDA 510(k) clearance?

CURITY SPINAL ANESTHESIA TRAY received FDA 510(k) clearance on 1990-12-19, under 510(k) number K903761.

Who is the listed applicant for CURITY SPINAL ANESTHESIA TRAY?

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 CURITY SPINAL ANESTHESIA TRAY?

The FDA product code for CURITY SPINAL ANESTHESIA TRAY 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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