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FDA 510(k)

KENDALL CURITY URETERAL CATHETER

K-Number: K964899 · 1997-02-07

ApplicantKendall Healthcare Products Co. Div.Of Tyco Health
Decision Date1997-02-07
Product CodeEYB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KENDALL CURITY URETERAL CATHETER 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 1997-02-07 under 510(k) number K964899. The device is classified under product code EYB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KENDALL CURITY URETERAL CATHETER?

KENDALL CURITY URETERAL CATHETER is a medical device that received FDA 510(k) clearance on 1997-02-07. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K964899.

When did KENDALL CURITY URETERAL CATHETER receive FDA 510(k) clearance?

KENDALL CURITY URETERAL CATHETER received FDA 510(k) clearance on 1997-02-07, under 510(k) number K964899.

Who is the listed applicant for KENDALL CURITY URETERAL CATHETER?

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 KENDALL CURITY URETERAL CATHETER?

The FDA product code for KENDALL CURITY URETERAL CATHETER is EYB.

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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

View all 66 devices →

Related Devices (Code: EYB)

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.

K192183RocaTub Ureteral CatheterPromepal SamK191187Dornier MINNOW Ureteral CatheterDornier Medtech America, Inc.K183323UPJ Occlusion Balloon CatheterCook IncorporatedK182695Pigtail Ureteral Catheter Set, Sof-Flex AQ Coated Pigtail Ureteral CatheterCook IncorporatedK182122Ureteric CathetersColoplast Corp.K180182Dual Lumen Ureteral Access Catheter, Flexi-Tip Dual Lumen Ureteral Access CatheterCook Incorporated

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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