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)

CURITY RIG FOLEY CATH TRAY

K-Number: K841169 · 1984-07-06

Decision Date1984-07-06
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CURITY RIG FOLEY CATH TRAY is the device name listed in this FDA 510(k) record. The listed applicant is The Kendal Co.. It received FDA 510(k) clearance on 1984-07-06 under 510(k) number K841169. 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 CURITY RIG FOLEY CATH TRAY?

CURITY RIG FOLEY CATH TRAY is a medical device that received FDA 510(k) clearance on 1984-07-06. The listed applicant is The Kendal Co.. The 510(k) number is K841169.

When did CURITY RIG FOLEY CATH TRAY receive FDA 510(k) clearance?

CURITY RIG FOLEY CATH TRAY received FDA 510(k) clearance on 1984-07-06, under 510(k) number K841169.

Who is the listed applicant for CURITY RIG FOLEY CATH TRAY?

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

What is the FDA product code for CURITY RIG FOLEY CATH TRAY?

The FDA product code for CURITY RIG FOLEY CATH TRAY 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 Kendal 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 63 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.

↑