Ready to use Nelaton Catheter
K-Number: K251178 · 2026-01-02
ApplicantJamjoom Fullcare Corporation
Decision Date2026-01-02
Product CodeEZD
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Ready to use Nelaton Catheter is a medical device manufactured by Jamjoom Fullcare Corporation. It received FDA 510(k) clearance on 2026-01-02 under approval number K251178. 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 Ready to use Nelaton Catheter?
Ready to use Nelaton Catheter is a medical device that received FDA 510(k) clearance on 2026-01-02. It is manufactured by Jamjoom Fullcare Corporation. The 510(k) number is K251178.
When was Ready to use Nelaton Catheter approved by the FDA?
Ready to use Nelaton Catheter received FDA 510(k) clearance on 2026-01-02, under approval number K251178.
What company makes Ready to use Nelaton Catheter?
Ready to use Nelaton Catheter is manufactured by Jamjoom Fullcare Corporation.
What is the FDA product code for Ready to use Nelaton Catheter?
The FDA product code for Ready to use Nelaton Catheter is EZD.
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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.