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FDA 510(k)

CONVEEN(R) NIGHT DRAINAGE BAG (2000 ML)

K-Number: K871610 · 1987-06-10

ApplicantColoplast A/S
Decision Date1987-06-10
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CONVEEN(R) NIGHT DRAINAGE BAG (2000 ML) is the device name listed in this FDA 510(k) record. The listed applicant is Coloplast A/S. It received FDA 510(k) clearance on 1987-06-10 under 510(k) number K871610. The device is classified under product code KNX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONVEEN(R) NIGHT DRAINAGE BAG (2000 ML)?

CONVEEN(R) NIGHT DRAINAGE BAG (2000 ML) is a medical device that received FDA 510(k) clearance on 1987-06-10. The listed applicant is Coloplast A/S. The 510(k) number is K871610.

When did CONVEEN(R) NIGHT DRAINAGE BAG (2000 ML) receive FDA 510(k) clearance?

CONVEEN(R) NIGHT DRAINAGE BAG (2000 ML) received FDA 510(k) clearance on 1987-06-10, under 510(k) number K871610.

Who is the listed applicant for CONVEEN(R) NIGHT DRAINAGE BAG (2000 ML)?

The FDA 510(k) record lists Coloplast A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONVEEN(R) NIGHT DRAINAGE BAG (2000 ML)?

The FDA product code for CONVEEN(R) NIGHT DRAINAGE BAG (2000 ML) is KNX.

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.

Other records listing Coloplast A/S 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.

View all 66 devices →

Related Devices (Code: KNX)

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.

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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