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FDA 510(k)

CURITY PERCUTANEOUS CATHETER INSERTION KIT

K-Number: K855061 · 1986-04-16

ApplicantThe Kendal Co.
Decision Date1986-04-16
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CURITY PERCUTANEOUS CATHETER INSERTION 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 1986-04-16 under 510(k) number K855061. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURITY PERCUTANEOUS CATHETER INSERTION KIT?

CURITY PERCUTANEOUS CATHETER INSERTION KIT is a medical device that received FDA 510(k) clearance on 1986-04-16. The listed applicant is The Kendal Co.. The 510(k) number is K855061.

When did CURITY PERCUTANEOUS CATHETER INSERTION KIT receive FDA 510(k) clearance?

CURITY PERCUTANEOUS CATHETER INSERTION KIT received FDA 510(k) clearance on 1986-04-16, under 510(k) number K855061.

Who is the listed applicant for CURITY PERCUTANEOUS CATHETER INSERTION 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 PERCUTANEOUS CATHETER INSERTION KIT?

The FDA product code for CURITY PERCUTANEOUS CATHETER INSERTION KIT is DYB.

Related Clinical Trials

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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: DYB)

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.

K253526NAMIC Dilator and SheathMedline Industries, LPK261529Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set/ Microintroducer Kit / Microintroducer Kit (SIS05C); Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set / Microintroducer Kit / Microintroducer Kit (IS01); Introducer Kit / Microintroducer Kit / Introducer Set /Microintroducer Set / Micro Introducer Sheath Set / Introducer Sheath Set (NIS04)Hartman Medical Group, LLCK261242SimplGuidePendracareK261950Health Line Tearaway IntroducerHealth Line International CorporationK261492FieldFlex Steerable SheathCenterPoint Systems, LLCK260606Echo Large Bore Introducer SheathEcho Medical, LLC

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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