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FDA 510(k)

THE NEEDLE CATCHER

K-Number: K051281 · 2005-09-08

ApplicantE.D.Medical , Ltd.
Decision Date2005-09-08
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

THE NEEDLE CATCHER is the device name listed in this FDA 510(k) record. The listed applicant is E.D.Medical , Ltd.. It received FDA 510(k) clearance on 2005-09-08 under 510(k) number K051281. The device is classified under product code HTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE NEEDLE CATCHER?

THE NEEDLE CATCHER is a medical device that received FDA 510(k) clearance on 2005-09-08. The listed applicant is E.D.Medical , Ltd.. The 510(k) number is K051281.

When did THE NEEDLE CATCHER receive FDA 510(k) clearance?

THE NEEDLE CATCHER received FDA 510(k) clearance on 2005-09-08, under 510(k) number K051281.

Who is the listed applicant for THE NEEDLE CATCHER?

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

What is the FDA product code for THE NEEDLE CATCHER?

The FDA product code for THE NEEDLE CATCHER is HTD.

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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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