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FDA 510(k)

Ez Catch Auto; Ez Catch YR; Ez Catch TR

K-Number: K240205 · 2024-04-15

ApplicantVeol Medical Technologies Pvt , Ltd.
Decision Date2024-04-15
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Ez Catch Auto; Ez Catch YR; Ez Catch TR is the device name listed in this FDA 510(k) record. The listed applicant is Veol Medical Technologies Pvt , Ltd.. It received FDA 510(k) clearance on 2024-04-15 under 510(k) number K240205. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ez Catch Auto; Ez Catch YR; Ez Catch TR?

Ez Catch Auto; Ez Catch YR; Ez Catch TR is a medical device that received FDA 510(k) clearance on 2024-04-15. The listed applicant is Veol Medical Technologies Pvt , Ltd.. The 510(k) number is K240205.

When did Ez Catch Auto; Ez Catch YR; Ez Catch TR receive FDA 510(k) clearance?

Ez Catch Auto; Ez Catch YR; Ez Catch TR received FDA 510(k) clearance on 2024-04-15, under 510(k) number K240205.

Who is the listed applicant for Ez Catch Auto; Ez Catch YR; Ez Catch TR?

The FDA 510(k) record lists Veol Medical Technologies Pvt , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ez Catch Auto; Ez Catch YR; Ez Catch TR?

The FDA product code for Ez Catch Auto; Ez Catch YR; Ez Catch TR is GCJ.

Other records listing Veol Medical Technologies Pvt , Ltd. 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.

K241595EzVu Visual Vasopressor injector (EV-19)

Related Devices (Code: GCJ)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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