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)

TRIBAG, TRIBAND & TRIFIX-REUSEABLE URINE COLLECTOR

K-Number: K851471 · 1985-06-12

ApplicantLic-Orthion
Decision Date1985-06-12
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TRIBAG, TRIBAND & TRIFIX-REUSEABLE URINE COLLECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Lic-Orthion. It received FDA 510(k) clearance on 1985-06-12 under 510(k) number K851471. 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 TRIBAG, TRIBAND & TRIFIX-REUSEABLE URINE COLLECTOR?

TRIBAG, TRIBAND & TRIFIX-REUSEABLE URINE COLLECTOR is a medical device that received FDA 510(k) clearance on 1985-06-12. The listed applicant is Lic-Orthion. The 510(k) number is K851471.

When did TRIBAG, TRIBAND & TRIFIX-REUSEABLE URINE COLLECTOR receive FDA 510(k) clearance?

TRIBAG, TRIBAND & TRIFIX-REUSEABLE URINE COLLECTOR received FDA 510(k) clearance on 1985-06-12, under 510(k) number K851471.

Who is the listed applicant for TRIBAG, TRIBAND & TRIFIX-REUSEABLE URINE COLLECTOR?

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

What is the FDA product code for TRIBAG, TRIBAND & TRIFIX-REUSEABLE URINE COLLECTOR?

The FDA product code for TRIBAG, TRIBAND & TRIFIX-REUSEABLE URINE COLLECTOR 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 Lic-Orthion 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 17 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.

↑