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FDA 510(k)

GESCO DUAL LUMEN UMBILICATH II-DL

K-Number: K896041 · 1990-04-17

ApplicantGesco Intl., Inc.
Decision Date1990-04-17
Product CodeFOS
Advisory CommitteeHO
DecisionUnknown

Device Summary

GESCO DUAL LUMEN UMBILICATH II-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 1990-04-17 under 510(k) number K896041. The device is classified under product code FOS. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the GESCO DUAL LUMEN UMBILICATH II-DL?

GESCO DUAL LUMEN UMBILICATH II-DL is a medical device that received FDA 510(k) clearance on 1990-04-17. The listed applicant is Gesco Intl., Inc.. The 510(k) number is K896041.

When did GESCO DUAL LUMEN UMBILICATH II-DL receive FDA 510(k) clearance?

GESCO DUAL LUMEN UMBILICATH II-DL received FDA 510(k) clearance on 1990-04-17, under 510(k) number K896041.

Who is the listed applicant for GESCO DUAL LUMEN UMBILICATH II-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 UMBILICATH II-DL?

The FDA product code for GESCO DUAL LUMEN UMBILICATH II-DL is FOS.

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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: FOS)

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.

K201697Umbilical Vessels CatheterHaolang Medical USA CorporationK130725MODIFIED ARGYLE POLYURETHANE UMBILICAL VESSEL CATHETER 2.5FR, 3.5FR, 5 FR.Covidien Lp, Formerly Registered AS KendallK120304FOOTPRINT MEDICAL POLYURETHANE UMBILICAL CATHETERFootprint Medical, Inc.K091214FOOTPRINT MEDICAL SILICONE UMBILICAL CATHETERFootprint MedicalK091213FOOTPRINT MEDICAL UMBILICAL CATHETER, DUAL LUMENFootprint MedicalK081515NEOMED DUAL LUMEN UMBILICAL CATHETER, MODELS S2UVC4.0, S2UVC5.0Neomed, 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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