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FDA 510(k)

CATH TRAY W/OUT CATHETER

K-Number: K780267 · 1978-02-24

ApplicantLatex Ind., Inc.
Decision Date1978-02-24
Product CodeEYZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATH TRAY W/OUT CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Latex Ind., Inc.. It received FDA 510(k) clearance on 1978-02-24 under 510(k) number K780267. The device is classified under product code EYZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATH TRAY W/OUT CATHETER?

CATH TRAY W/OUT CATHETER is a medical device that received FDA 510(k) clearance on 1978-02-24. The listed applicant is Latex Ind., Inc.. The 510(k) number is K780267.

When did CATH TRAY W/OUT CATHETER receive FDA 510(k) clearance?

CATH TRAY W/OUT CATHETER received FDA 510(k) clearance on 1978-02-24, under 510(k) number K780267.

Who is the listed applicant for CATH TRAY W/OUT CATHETER?

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

What is the FDA product code for CATH TRAY W/OUT CATHETER?

The FDA product code for CATH TRAY W/OUT CATHETER is EYZ.

Related Clinical Trials

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.

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Other records listing Latex Ind., 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.

K812058AKRON URINARY DRAINAGE BATK810281UROLOGICAL CATHETERSK791674BLADDER RETENTION CATHETERIZATION TRAYK781751CATHETER, AKRON FOLEY TEFLONK781433AKRON MALE EXTERNAL CATHETERK772277BLADDER RETENTION-CATHETHERIZATIONTRAY

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Related Devices (Code: EYZ)

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.

K964219ZIP CONDOM CATHETERGoulter Medical, Inc.K961906UNI-GARD QUIK CATH(SIZES 8 FRENCH THROUGH 18)UG 10008,10010,10012,10014,10016,10018Spectrum Medsystems Corp.K952780URINARY GEL DRAINAGE SYSTEMP.A.M., Inc.K951597URINARY DRAINAGE BAGKey Medical Services, Inc.K942753ONE STEP SPECIMEN COLLECTOR/TRANSPORT CONTAINERResearched, Novel Medical Devices (Rn/Md)K933126COMFORTCARE SYSTEMPatsy J. Trisler, J.D.

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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