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FDA 510(k)

EXEL INDWELLING CATHETER

K-Number: K895772 · 1990-02-16

ApplicantExel Intl.
Decision Date1990-02-16
Product CodeFDZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EXEL INDWELLING CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Exel Intl.. It received FDA 510(k) clearance on 1990-02-16 under 510(k) number K895772. The device is classified under product code FDZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXEL INDWELLING CATHETER?

EXEL INDWELLING CATHETER is a medical device that received FDA 510(k) clearance on 1990-02-16. The listed applicant is Exel Intl.. The 510(k) number is K895772.

When did EXEL INDWELLING CATHETER receive FDA 510(k) clearance?

EXEL INDWELLING CATHETER received FDA 510(k) clearance on 1990-02-16, under 510(k) number K895772.

Who is the listed applicant for EXEL INDWELLING CATHETER?

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

What is the FDA product code for EXEL INDWELLING CATHETER?

The FDA product code for EXEL INDWELLING CATHETER is FDZ.

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Other records listing Exel Intl. 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.

K992290EXEL INJECTION PLUG WITH CAPK963658EXEL AVF SINGLE NEEDLEK963659EXEL I.V. ADMINISTRATION SETK926119EXEL HUBER INFUSION SET ROTATING WINGK904685EXEL HUBER INFUSION SET WITHOUT INJECTION SITE (Y)K903945EXEL A-V FISTULA SET

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Related Devices (Code: FDZ)

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.

K852642CENTRAL VEIN CATHETERIZATION TRAYTeleflexmedical, Inc.

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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