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FDA 510(k)

CURITY VENOUS CATHETERIZATION KIT

K-Number: K861828 · 1986-07-10

ApplicantThe Kendal Co.
Decision Date1986-07-10
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CURITY VENOUS CATHETERIZATION KIT 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 1986-07-10 under 510(k) number K861828. 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 VENOUS CATHETERIZATION KIT?

CURITY VENOUS CATHETERIZATION KIT is a medical device that received FDA 510(k) clearance on 1986-07-10. The listed applicant is The Kendal Co.. The 510(k) number is K861828.

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

CURITY VENOUS CATHETERIZATION KIT received FDA 510(k) clearance on 1986-07-10, under 510(k) number K861828.

Who is the listed applicant for CURITY VENOUS CATHETERIZATION KIT?

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 VENOUS CATHETERIZATION KIT?

The FDA product code for CURITY VENOUS CATHETERIZATION KIT 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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