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

FDA 510(k)

FULL CARE Disposable PVC Nelaton Catheter

K-Number: K151745 · 2016-03-03

Decision Date2016-03-03
Product CodeEZD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FULL CARE Disposable PVC Nelaton Catheter is a medical device manufactured by Shaoxing Fuqing Health Products Co., Ltd.. It received FDA 510(k) clearance on 2016-03-03 under approval number K151745. The device is classified under product code EZD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FULL CARE Disposable PVC Nelaton Catheter?

FULL CARE Disposable PVC Nelaton Catheter is a medical device that received FDA 510(k) clearance on 2016-03-03. It is manufactured by Shaoxing Fuqing Health Products Co., Ltd.. The 510(k) number is K151745.

When was FULL CARE Disposable PVC Nelaton Catheter approved by the FDA?

FULL CARE Disposable PVC Nelaton Catheter received FDA 510(k) clearance on 2016-03-03, under approval number K151745.

What company makes FULL CARE Disposable PVC Nelaton Catheter?

FULL CARE Disposable PVC Nelaton Catheter is manufactured by Shaoxing Fuqing Health Products Co., Ltd..

What is the FDA product code for FULL CARE Disposable PVC Nelaton Catheter?

The FDA product code for FULL CARE Disposable PVC Nelaton Catheter is EZD.

Related Clinical Trials

Related Devices (Code: EZD)

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.