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FDA 510(k)

CURITY CENTRAL VENOUS CATHETERIZATION TRAY

K-Number: K861827 · 1986-07-11

ApplicantThe Kendal Co.
Decision Date1986-07-11
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CURITY CENTRAL VENOUS CATHETERIZATION 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 1986-07-11 under 510(k) number K861827. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURITY CENTRAL VENOUS CATHETERIZATION TRAY?

CURITY CENTRAL VENOUS CATHETERIZATION TRAY is a medical device that received FDA 510(k) clearance on 1986-07-11. The listed applicant is The Kendal Co.. The 510(k) number is K861827.

When did CURITY CENTRAL VENOUS CATHETERIZATION TRAY receive FDA 510(k) clearance?

CURITY CENTRAL VENOUS CATHETERIZATION TRAY received FDA 510(k) clearance on 1986-07-11, under 510(k) number K861827.

Who is the listed applicant for CURITY CENTRAL VENOUS CATHETERIZATION 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 CENTRAL VENOUS CATHETERIZATION TRAY?

The FDA product code for CURITY CENTRAL VENOUS CATHETERIZATION TRAY is DQY.

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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: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

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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