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FDA 510(k)

GESCO CATHETERIZATION TRAY

K-Number: K882647 · 1988-09-09

ApplicantGesco Intl., Inc.
Decision Date1988-09-09
Product CodeGBQ
Advisory CommitteeSU
DecisionUnknown

Device Summary

GESCO CATHETERIZATION TRAY 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 1988-09-09 under 510(k) number K882647. The device is classified under product code GBQ. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the GESCO CATHETERIZATION TRAY?

GESCO CATHETERIZATION TRAY is a medical device that received FDA 510(k) clearance on 1988-09-09. The listed applicant is Gesco Intl., Inc.. The 510(k) number is K882647.

When did GESCO CATHETERIZATION TRAY receive FDA 510(k) clearance?

GESCO CATHETERIZATION TRAY received FDA 510(k) clearance on 1988-09-09, under 510(k) number K882647.

Who is the listed applicant for GESCO CATHETERIZATION TRAY?

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 CATHETERIZATION TRAY?

The FDA product code for GESCO CATHETERIZATION TRAY is GBQ.

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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-LINEK940870UMBILI-CATHK940953UMBILI-CATH-SK940952UMBILI-CATH-S-DLK941672URI-CATH CATHETERK941232THORA-CATH

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Related Devices (Code: GBQ)

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.

K941356MICROFLOW IRRIGATION SYSTEMJedmed Instrument Co.K921464CAT.#40100, 40102, 40104 & 40106 YANKAUER SUCT INTTrinity Laboratories, Inc.K874596PERFORATED SOAKING TUBESpecialty Medical Products Co.K873097PROCEDUAL CHANGES/ASSEMBLY PROCESS FOR PLUS PAKSIpax, Inc.K872787MODIFIED CURLCATHQuinton, Inc.K791400GASTRIC LAVAGE KIT-DISPOSABLEAcumed Instruments Corp.

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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