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FDA 510(k)

CORPAK URINARY DRAINAGE BAG

K-Number: K842257 · 1984-08-08

ApplicantCorpak Co.
Decision Date1984-08-08
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CORPAK URINARY DRAINAGE BAG is the device name listed in this FDA 510(k) record. The listed applicant is Corpak Co.. It received FDA 510(k) clearance on 1984-08-08 under 510(k) number K842257. 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 CORPAK URINARY DRAINAGE BAG?

CORPAK URINARY DRAINAGE BAG is a medical device that received FDA 510(k) clearance on 1984-08-08. The listed applicant is Corpak Co.. The 510(k) number is K842257.

When did CORPAK URINARY DRAINAGE BAG receive FDA 510(k) clearance?

CORPAK URINARY DRAINAGE BAG received FDA 510(k) clearance on 1984-08-08, under 510(k) number K842257.

Who is the listed applicant for CORPAK URINARY DRAINAGE BAG?

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

What is the FDA product code for CORPAK URINARY DRAINAGE BAG?

The FDA product code for CORPAK URINARY DRAINAGE BAG 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 Corpak Co. 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 21 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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