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FDA 510(k)

CURITY CONTINUOUS EPIDURAL ANESTHESIA TRAY

K-Number: K871066 · 1987-05-15

ApplicantThe Kendal Co.
Decision Date1987-05-15
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CURITY CONTINUOUS EPIDURAL ANESTHESIA TRAY is the device name listed in this FDA 510(k) record. The listed applicant is The Kendal Co.. It received FDA 510(k) clearance on 1987-05-15 under 510(k) number K871066. 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 CONTINUOUS EPIDURAL ANESTHESIA TRAY?

CURITY CONTINUOUS EPIDURAL ANESTHESIA TRAY is a medical device that received FDA 510(k) clearance on 1987-05-15. The listed applicant is The Kendal Co.. The 510(k) number is K871066.

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

CURITY CONTINUOUS EPIDURAL ANESTHESIA TRAY received FDA 510(k) clearance on 1987-05-15, under 510(k) number K871066.

Who is the listed applicant for CURITY CONTINUOUS EPIDURAL ANESTHESIA TRAY?

The FDA 510(k) record lists The Kendal Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CURITY CONTINUOUS EPIDURAL ANESTHESIA TRAY?

The FDA product code for CURITY CONTINUOUS EPIDURAL ANESTHESIA TRAY is CAZ.

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Other records listing The Kendal Co. 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.

K000087MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FRK990500KENDALL ULTRAMER COUDE FOLEY CATHETER, MODEL 1416C, KENDALL CURITY COUDE FOLEY CATHETER TRAY, MODEL 6946CK991758MONOJECT INSULIN SYRINGEK970969KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SETK951488KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAPK942664KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM

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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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