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FDA 510(k)

VPI NON-ADHESIVE CONDOM CATHETER

K-Number: K883119 · 1988-08-02

ApplicantCook Urological, Inc.
Decision Date1988-08-02
Product CodeEYT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VPI NON-ADHESIVE CONDOM CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Cook Urological, Inc.. It received FDA 510(k) clearance on 1988-08-02 under 510(k) number K883119. The device is classified under product code EYT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VPI NON-ADHESIVE CONDOM CATHETER?

VPI NON-ADHESIVE CONDOM CATHETER is a medical device that received FDA 510(k) clearance on 1988-08-02. The listed applicant is Cook Urological, Inc.. The 510(k) number is K883119.

When did VPI NON-ADHESIVE CONDOM CATHETER receive FDA 510(k) clearance?

VPI NON-ADHESIVE CONDOM CATHETER received FDA 510(k) clearance on 1988-08-02, under 510(k) number K883119.

Who is the listed applicant for VPI NON-ADHESIVE CONDOM CATHETER?

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

What is the FDA product code for VPI NON-ADHESIVE CONDOM CATHETER?

The FDA product code for VPI NON-ADHESIVE CONDOM CATHETER is EYT.

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Other records listing Cook Urological, Inc. as applicant

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Related Devices (Code: EYT)

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K934080URINARY DRAINAGE BAGKit Pak, Inc.K935774CURITY FAST-CATH FEMALE CATHETER KITKendall Healthcare Products Co. Div.Of Tyco HealthK883057COMFORT CATH MALE EXTERNAL CATHETERSierra Laboratories, 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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