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FDA 510(k)

COLOSTOMY DEVICE W/ PRESSURE LID

K-Number: K790750 · 1979-05-14

ApplicantVabar Corp.
Decision Date1979-05-14
Product CodeEXD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

COLOSTOMY DEVICE W/ PRESSURE LID is the device name listed in this FDA 510(k) record. The listed applicant is Vabar Corp.. It received FDA 510(k) clearance on 1979-05-14 under 510(k) number K790750. The device is classified under product code EXD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLOSTOMY DEVICE W/ PRESSURE LID?

COLOSTOMY DEVICE W/ PRESSURE LID is a medical device that received FDA 510(k) clearance on 1979-05-14. The listed applicant is Vabar Corp.. The 510(k) number is K790750.

When did COLOSTOMY DEVICE W/ PRESSURE LID receive FDA 510(k) clearance?

COLOSTOMY DEVICE W/ PRESSURE LID received FDA 510(k) clearance on 1979-05-14, under 510(k) number K790750.

Who is the listed applicant for COLOSTOMY DEVICE W/ PRESSURE LID?

The FDA 510(k) record lists Vabar Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COLOSTOMY DEVICE W/ PRESSURE LID?

The FDA product code for COLOSTOMY DEVICE W/ PRESSURE LID is EXD.

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 Vabar Corp. 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.

K790749COLOSTOMY ENEMA DEVICE

Related Devices (Code: EXD)

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.

K121833OSTOMY IRRIGATION SETColoplast A/SK914692URINARY DIVERSION EVACUATING CATHETERCook Urological, Inc.K904586PALEX IRRIGATION SETPalex Intl. SAK871791BLOXOM IRRIGATORI.B. Bloxom C/O Hogan & HartsonK840268IRRIGATION SYSTEMColoplast A/SK832299VISI-FLOW IRRIGATORConvatec, A Division of E.R. Squibb & Sons

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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