Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

URINARY COLLECTION CONTAINER/LEG BAG

K-Number: K821171 · 1982-05-10

Decision Date1982-05-10
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

URINARY COLLECTION CONTAINER/LEG BAG is the device name listed in this FDA 510(k) record. The listed applicant is The Healthcare Group Laboratories, Inc.. It received FDA 510(k) clearance on 1982-05-10 under 510(k) number K821171. 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 URINARY COLLECTION CONTAINER/LEG BAG?

URINARY COLLECTION CONTAINER/LEG BAG is a medical device that received FDA 510(k) clearance on 1982-05-10. The listed applicant is The Healthcare Group Laboratories, Inc.. The 510(k) number is K821171.

When did URINARY COLLECTION CONTAINER/LEG BAG receive FDA 510(k) clearance?

URINARY COLLECTION CONTAINER/LEG BAG received FDA 510(k) clearance on 1982-05-10, under 510(k) number K821171.

Who is the listed applicant for URINARY COLLECTION CONTAINER/LEG BAG?

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

What is the FDA product code for URINARY COLLECTION CONTAINER/LEG BAG?

The FDA product code for URINARY COLLECTION CONTAINER/LEG 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 The Healthcare Group Laboratories, Inc. 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 29 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.

↑