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FDA 510(k)

BANGORT LIFESTYLE COLOSTOMY POUCHES

K-Number: K841029 · 1984-04-04

ApplicantHowmedica Corp.
Decision Date1984-04-04
Product CodeEXB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BANGORT LIFESTYLE COLOSTOMY POUCHES is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1984-04-04 under 510(k) number K841029. The device is classified under product code EXB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BANGORT LIFESTYLE COLOSTOMY POUCHES?

BANGORT LIFESTYLE COLOSTOMY POUCHES is a medical device that received FDA 510(k) clearance on 1984-04-04. The listed applicant is Howmedica Corp.. The 510(k) number is K841029.

When did BANGORT LIFESTYLE COLOSTOMY POUCHES receive FDA 510(k) clearance?

BANGORT LIFESTYLE COLOSTOMY POUCHES received FDA 510(k) clearance on 1984-04-04, under 510(k) number K841029.

Who is the listed applicant for BANGORT LIFESTYLE COLOSTOMY POUCHES?

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

What is the FDA product code for BANGORT LIFESTYLE COLOSTOMY POUCHES?

The FDA product code for BANGORT LIFESTYLE COLOSTOMY POUCHES is EXB.

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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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