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FDA 510(k)

GESCO DUAL LUMEN PER-Q-CATH-DL

K-Number: K895942 · 1990-07-02

ApplicantGesco Intl., Inc.
Decision Date1990-07-02
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GESCO DUAL LUMEN PER-Q-CATH-DL is the device name listed in this FDA 510(k) record. The listed applicant is Gesco Intl., Inc.. It received FDA 510(k) clearance on 1990-07-02 under 510(k) number K895942. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GESCO DUAL LUMEN PER-Q-CATH-DL?

GESCO DUAL LUMEN PER-Q-CATH-DL is a medical device that received FDA 510(k) clearance on 1990-07-02. The listed applicant is Gesco Intl., Inc.. The 510(k) number is K895942.

When did GESCO DUAL LUMEN PER-Q-CATH-DL receive FDA 510(k) clearance?

GESCO DUAL LUMEN PER-Q-CATH-DL received FDA 510(k) clearance on 1990-07-02, under 510(k) number K895942.

Who is the listed applicant for GESCO DUAL LUMEN PER-Q-CATH-DL?

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

What is the FDA product code for GESCO DUAL LUMEN PER-Q-CATH-DL?

The FDA product code for GESCO DUAL LUMEN PER-Q-CATH-DL is FOZ.

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Other records listing Gesco Intl., Inc. 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.

K954422PER-Q-CATH MID-LINEK940953UMBILI-CATH-SK940870UMBILI-CATHK940952UMBILI-CATH-S-DLK941672URI-CATH CATHETERK941232THORA-CATH

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Related Devices (Code: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, 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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