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FDA 510(k)

GREENLIGHT 300

K-Number: K040410 · 2004-05-05

ApplicantA C Cossor & Son (Surgical) Limited
Decision Date2004-05-05
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

GREENLIGHT 300 is the device name listed in this FDA 510(k) record. The listed applicant is A C Cossor & Son (Surgical) Limited. It received FDA 510(k) clearance on 2004-05-05 under 510(k) number K040410. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GREENLIGHT 300?

GREENLIGHT 300 is a medical device that received FDA 510(k) clearance on 2004-05-05. The listed applicant is A C Cossor & Son (Surgical) Limited. The 510(k) number is K040410.

When did GREENLIGHT 300 receive FDA 510(k) clearance?

GREENLIGHT 300 received FDA 510(k) clearance on 2004-05-05, under 510(k) number K040410.

Who is the listed applicant for GREENLIGHT 300?

The FDA 510(k) record lists A C Cossor & Son (Surgical) Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GREENLIGHT 300?

The FDA product code for GREENLIGHT 300 is DXN.

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Related Devices (Code: DXN)

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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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